Thursday, 29 September 2016

Miscellaneous antipsychotic agents


A drug may be classified by the chemical type of the active ingredient or by the way it is used to treat a particular condition. Each drug can be classified into one or more drug classes.

Miscellaneous antipsychotics are agents that have different modes of action to treat schizophrenia and other mood disorders. They are slightly different to the typical and atypical antipsychotics.

See also

Medical conditions associated with miscellaneous antipsychotic agents:

  • Bipolar Disorder
  • Cluster Headaches
  • Dementia
  • ICU Agitation
  • Mania
  • Nausea/Vomiting
  • Psychosis
  • Schizoaffective Disorder
  • Schizophrenia
  • Tourette's Syndrome

Drug List:

Flumazénil Dakota Pharm




Flumazénil Dakota Pharm may be available in the countries listed below.


Ingredient matches for Flumazénil Dakota Pharm



Flumazenil

Flumazenil is reported as an ingredient of Flumazénil Dakota Pharm in the following countries:


  • France

International Drug Name Search

Hi-Tac




Hi-Tac may be available in the countries listed below.


Ingredient matches for Hi-Tac



Ranitidine

Ranitidine hydrochloride (a derivative of Ranitidine) is reported as an ingredient of Hi-Tac in the following countries:


  • Bangladesh

International Drug Name Search

Suldimet




Suldimet may be available in the countries listed below.


In some countries, this medicine may only be approved for veterinary use.

Ingredient matches for Suldimet



Sulfadimethoxine

Sulfadimethoxine is reported as an ingredient of Suldimet in the following countries:


  • Italy

International Drug Name Search

Wednesday, 28 September 2016

Morphine HCl EG




Morphine HCl EG may be available in the countries listed below.


Ingredient matches for Morphine HCl EG



Morphine

Morphine hydrochloride (a derivative of Morphine) is reported as an ingredient of Morphine HCl EG in the following countries:


  • Luxembourg

International Drug Name Search

Intagenta




Intagenta may be available in the countries listed below.


Ingredient matches for Intagenta



Gentamicin

Gentamicin is reported as an ingredient of Intagenta in the following countries:


  • Peru

Gentamicin sulfate (a derivative of Gentamicin) is reported as an ingredient of Intagenta in the following countries:


  • Ethiopia

International Drug Name Search

Spasmoson




Spasmoson may be available in the countries listed below.


Ingredient matches for Spasmoson



Scopolamine

Scopolamine is reported as an ingredient of Spasmoson in the following countries:


  • Bangladesh

International Drug Name Search

Solvolan




Solvolan may be available in the countries listed below.


Ingredient matches for Solvolan



Ambroxol

Ambroxol hydrochloride (a derivative of Ambroxol) is reported as an ingredient of Solvolan in the following countries:


  • Bulgaria

  • Czech Republic

  • Slovakia

  • Slovenia

International Drug Name Search

Remeron SolTab Orally Disintegrating Tablets


Pronunciation: mir-TAZ-a-peen
Generic Name: Mirtazapine
Brand Name: Remeron SolTab

Antidepressants may increase the risk of suicidal thoughts or actions in children, teenagers, and young adults. However, depression and certain other mental problems may also increase the risk of suicide. Talk with the patient's doctor to be sure that the benefits of using Remeron SolTab Orally Disintegrating Tablets outweigh the risks.


Families and caregivers must closely watch patients who take Remeron SolTab Orally Disintegrating Tablets. It is important to keep in close contact with the patient's doctor. Tell the doctor right away if the patient has symptoms like worsened depression, suicidal thoughts, or changes in behavior. Discuss any questions with the patient's doctor.





Remeron SolTab Orally Disintegrating Tablets are used for:

Treating depression. It may also be used for other conditions as determined by your doctor.


Remeron SolTab Orally Disintegrating Tablets are a tetracyclic antidepressant. Exactly how Remeron SolTab Orally Disintegrating Tablets improves depression symptoms is not known. It is thought to increase the activity of certain chemicals in the brain (norepinephrine, serotonin) that help improve mood.


Do NOT use Remeron SolTab Orally Disintegrating Tablets if:


  • you are allergic to any ingredient in Remeron SolTab Orally Disintegrating Tablets

  • you are taking oxitriptan or tryptophan

  • you are taking or have taken furazolidone, linezolid, methylene blue, or a monoamine oxidase inhibitor (MAOI) (eg, phenelzine) within the last 14 days

Contact your doctor or health care provider right away if any of these apply to you.



Video: Treatment for Depression







Treatments for depression are getting better everyday and there are things you can start doing right away.






Before using Remeron SolTab Orally Disintegrating Tablets:


Some medical conditions may interact with Remeron SolTab Orally Disintegrating Tablets. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:


  • if you are pregnant, planning to become pregnant, or are breast-feeding

  • if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

  • if you have allergies to medicines, foods, or other substances

  • if you have liver problems, high cholesterol, kidney problems, heart problems, blood vessel problems, a low white blood cell count, or phenylketonuria (PKU)

  • if you have a history of dizziness or fainting, seizures, heart attack, angina (chest pain), or stroke

  • if you have low blood pressure, low blood volume, low blood sodium levels, or you are dehydrated

  • if you have a history of mental or mood problems (eg, depression, bipolar disorder) or suicidal thoughts or behaviors

  • if you take medicine to treat high blood pressure

Some MEDICINES MAY INTERACT with Remeron SolTab Orally Disintegrating Tablets. Tell your health care provider if you are taking any other medicines, especially any of the following:


  • Fluvoxamine, furazolidone, linezolid, lithium, MAOIs (eg, phenelzine), methylene blue, oxitriptan, selective serotonin reuptake inhibitors (SSRIs) (eg, fluoxetine), serotonin 5-HT1 receptor agonists (eg, sumatriptan), serotonin-norepinephrine reuptake inhibitors (SNRIs) (eg, venlafaxine), St. John's word, tramadol, tryptophan, or tricyclic antidepressants (eg, amitriptyline) because they may increase the risk of serotonin syndrome, including increased risk of restlessness, fever, excessive sweating, twitching, and seizures that can, rarely, be life-threatening

  • Azole antifungals (eg, ketoconazole), benzodiazepines (eg, diazepam), cimetidine, HIV protease inhibitors (eg, ritonavir), macrolide antibiotics (eg, erythromycin), or nefazodone because they may increase the risk of Remeron SolTab Orally Disintegrating Tablets's side effects

  • Carbamazepine, phenytoin, or rifampin because they may decrease Remeron SolTab Orally Disintegrating Tablets's effectiveness

  • Warfarin because the risk of its side effects may be increased by Remeron SolTab Orally Disintegrating Tablets

  • Clonidine because its effectiveness may be decreased by Remeron SolTab Orally Disintegrating Tablets

This may not be a complete list of all interactions that may occur. Ask your health care provider if Remeron SolTab Orally Disintegrating Tablets may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.


How to use Remeron SolTab Orally Disintegrating Tablets:


Use Remeron SolTab Orally Disintegrating Tablets as directed by your doctor. Check the label on the medicine for exact dosing instructions.


  • Remeron SolTab Orally Disintegrating Tablets comes with an extra patient information sheet called a Medication Guide. Read it carefully. Read it again each time you get Remeron SolTab Orally Disintegrating Tablets refilled.

  • Take Remeron SolTab Orally Disintegrating Tablets by mouth with or without food.

  • Take Remeron SolTab Orally Disintegrating Tablets in the evening before bedtime unless your doctor tells you otherwise.

  • Do not remove the blister from the outer pouch until you are ready to take Remeron SolTab Orally Disintegrating Tablets. Make sure that your hands are dry when you open the blister pack. Do not push the tablet through the foil. Peel back the foil on the blister pack and place the tablet on your tongue. The tablet dissolves quickly and can be swallowed with saliva. Remeron SolTab Orally Disintegrating Tablets may be taken with or without water. Take the tablet immediately after opening the blister pack. Do not store the removed tablet for future use.

  • Improvement should be noticed within 1 to 4 weeks of taking Remeron SolTab Orally Disintegrating Tablets.

  • Continue to take Remeron SolTab Orally Disintegrating Tablets even if you feel well. Do not miss any doses.

  • Do not suddenly stop taking Remeron SolTab Orally Disintegrating Tablets without checking with your doctor. Side effects may occur. They may include abnormal dreams, numbness or tingling, confusion, dizziness, fatigue, mental or mood changes (eg, agitation, anxiety), headache, nausea, sweating, tremor, or vomiting. If you need to stop taking Remeron SolTab Orally Disintegrating Tablets, your doctor will slowly lower your dose.

  • If you miss a dose of Remeron SolTab Orally Disintegrating Tablets, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Remeron SolTab Orally Disintegrating Tablets.



Important safety information:


  • Remeron SolTab Orally Disintegrating Tablets may cause drowsiness or dizziness. These effects may be worse if you take it with alcohol or certain medicines. Use Remeron SolTab Orally Disintegrating Tablets with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.

  • Do not drink alcohol while you are taking Remeron SolTab Orally Disintegrating Tablets.

  • Check with your doctor before you take medicines that may cause drowsiness (eg, sleep aids, muscle relaxers) while you are taking Remeron SolTab Orally Disintegrating Tablets; it may add to their effects. Ask your pharmacist if you have questions about which medicines may cause drowsiness.

  • Remeron SolTab Orally Disintegrating Tablets may cause dizziness, lightheadedness, or fainting; alcohol, hot weather, exercise, or fever may increase these effects. To prevent them, sit up or stand slowly, especially in the morning. Sit or lie down at the first sign of any of these effects.

  • Children, teenagers, and young adults who take Remeron SolTab Orally Disintegrating Tablets may be at increased risk for suicidal thoughts or actions. Watch all patients who take Remeron SolTab Orally Disintegrating Tablets closely. Contact the doctor at once if new, worsened, or sudden symptoms such as depressed mood; anxious, restless, or irritable behavior; panic attacks; or any unusual change in mood or behavior occur. Contact the doctor right away if any signs of suicidal thoughts or actions occur.

  • Some of these products contain phenylalanine. If you must have a diet that is low in phenylalanine, ask your pharmacist if it is in your product.

  • Serotonin syndrome is a possibly fatal syndrome that can be caused by Remeron SolTab Orally Disintegrating Tablets. Your risk may be greater if you take Remeron SolTab Orally Disintegrating Tablets with certain other medicines (eg, antidepressants, "triptans," MAOIs). Symptoms may include agitation; confusion; hallucinations; coma; irritability; fever; fast or irregular heartbeat; tremor; excessive sweating; rigid muscles; severe headache or dizziness; and nausea, vomiting, or diarrhea. Contact your doctor at once if you have any of these symptoms.

  • Lab tests, including liver function, kidney function, and complete blood cell counts, may be performed while you use Remeron SolTab Orally Disintegrating Tablets. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

  • Use Remeron SolTab Orally Disintegrating Tablets with caution in the ELDERLY; they may be more sensitive to its effects, especially drowsiness, confusion, or low blood sodium levels.

  • Remeron SolTab Orally Disintegrating Tablets should not be used in CHILDREN; safety and effectiveness in children have not been confirmed.

  • PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Remeron SolTab Orally Disintegrating Tablets while you are pregnant. It is not known if Remeron SolTab Orally Disintegrating Tablets are found in breast milk. If you are or will be breast-feeding while you use Remeron SolTab Orally Disintegrating Tablets, check with your doctor. Discuss any possible risks to your baby.


Possible side effects of Remeron SolTab Orally Disintegrating Tablets:


All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:



Abnormal dreams; abnormal thinking; constipation; dizziness; drowsiness; dry mouth; flu symptoms; increased appetite; weakness; weight gain.



Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); mouth sores; new or worsening agitation, panic attacks, aggressiveness, impulsiveness, irritability, hostility, exaggerated feeling of well-being, trouble sleeping, restlessness, or inability to sit still; red, swollen, blistered, or peeling skin; seizures; severe headache or dizziness; sluggishness; suicidal thoughts or actions; symptoms of infection (eg, fever, chills, sore throat); tremors; unusual or severe mental or mood changes; worsening of depression.



This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.


See also: Remeron SolTab side effects (in more detail)


If OVERDOSE is suspected:


Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include agitation; disorientation; drowsiness or deep sleep; fast heartbeat; impaired memory; loss of consciousness; rigid muscles; sluggishness.


Proper storage of Remeron SolTab Orally Disintegrating Tablets:

Store Remeron SolTab Orally Disintegrating Tablets at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Remeron SolTab Orally Disintegrating Tablets out of the reach of children and away from pets.


General information:


  • If you have any questions about Remeron SolTab Orally Disintegrating Tablets, please talk with your doctor, pharmacist, or other health care provider.

  • Remeron SolTab Orally Disintegrating Tablets are to be used only by the patient for whom it is prescribed. Do not share it with other people.

  • If your symptoms do not improve or if they become worse, check with your doctor.

  • Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Remeron SolTab Orally Disintegrating Tablets. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.



Issue Date: February 1, 2012

Database Edition 12.1.1.002

Copyright © 2012 Wolters Kluwer Health, Inc.

More Remeron SolTab resources


  • Remeron SolTab Side Effects (in more detail)
  • Remeron SolTab Use in Pregnancy & Breastfeeding
  • Drug Images
  • Remeron SolTab Drug Interactions
  • Remeron SolTab Support Group
  • 2 Reviews for Remeron SolTab - Add your own review/rating


Compare Remeron SolTab with other medications


  • Anxiety
  • Depression
  • Hot Flashes
  • Insomnia

Tuesday, 27 September 2016

nadroparin Subcutaneous


na-droe-PARE-in


Available Dosage Forms:


  • Solution

Pharmacologic Class: Low Molecular Weight Heparin


Uses For nadroparin

Nadroparin is used to prevent and treat deep vein thrombosis, a condition in which harmful blood clots form in the blood vessels of the legs. These blood clots can travel to the lungs and can become lodged in the blood vessels of the lungs, causing a condition called pulmonary embolism. Nadroparin is used for several days after surgery, while you are unable to walk. Nadroparin also is used to prevent blood clots from forming during hemodialysis.


nadroparin is available only with your doctor's prescription.


Before Using nadroparin


In deciding to use a medicine, the risks of taking the medicine must be weighed against the good it will do. This is a decision you and your doctor will make. For nadroparin, the following should be considered:


Allergies


Tell your doctor if you have ever had any unusual or allergic reaction to nadroparin or any other medicines. Also tell your health care professional if you have any other types of allergies, such as to foods, dyes, preservatives, or animals. For non-prescription products, read the label or package ingredients carefully.


Pediatric


Studies on nadroparin have been done only in adult patients and there is no specific information comparing use of nadroparin in children with use in other age groups.


Geriatric


nadroparin has been tested and has not been shown to cause different side effects or problems in older people than it does in younger adults.


Interactions with Medicines


Although certain medicines should not be used together at all, in other cases two different medicines may be used together even if an interaction might occur. In these cases, your doctor may want to change the dose, or other precautions may be necessary. When you are taking nadroparin, it is especially important that your healthcare professional know if you are taking any of the medicines listed below. The following interactions have been selected on the basis of their potential significance and are not necessarily all-inclusive.


Using nadroparin with any of the following medicines is usually not recommended, but may be required in some cases. If both medicines are prescribed together, your doctor may change the dose or how often you use one or both of the medicines.


  • Aceclofenac

  • Acemetacin

  • Alclofenac

  • Alteplase, Recombinant

  • Anistreplase

  • Antithrombin, Recombinant

  • Apazone

  • Benoxaprofen

  • Bromfenac

  • Bufexamac

  • Carprofen

  • Citalopram

  • Clometacin

  • Clonixin

  • Dexketoprofen

  • Diclofenac

  • Diflunisal

  • Dipyrone

  • Droxicam

  • Escitalopram

  • Etodolac

  • Etofenamate

  • Felbinac

  • Fenbufen

  • Fenoprofen

  • Fentiazac

  • Floctafenine

  • Flufenamic Acid

  • Fluoxetine

  • Flurbiprofen

  • Fluvoxamine

  • Ibuprofen

  • Indomethacin

  • Indoprofen

  • Isoxicam

  • Ketoprofen

  • Ketorolac

  • Lornoxicam

  • Meclofenamate

  • Mefenamic Acid

  • Meloxicam

  • Nabumetone

  • Naproxen

  • Niflumic Acid

  • Nimesulide

  • Oxaprozin

  • Oxyphenbutazone

  • Paroxetine

  • Phenylbutazone

  • Pirazolac

  • Piroxicam

  • Pirprofen

  • Propyphenazone

  • Proquazone

  • Reteplase, Recombinant

  • Sertraline

  • Streptokinase

  • Sulindac

  • Suprofen

  • Tenecteplase

  • Tenidap

  • Tenoxicam

  • Tiaprofenic Acid

  • Tolmetin

  • Urokinase

  • Zomepirac

Using nadroparin with any of the following medicines may cause an increased risk of certain side effects, but using both drugs may be the best treatment for you. If both medicines are prescribed together, your doctor may change the dose or how often you use one or both of the medicines.


  • Aspirin

  • Benorilate

  • Choline Magnesium Trisalicylate

  • Mesalamine

  • Olsalazine

  • Salicylamide

  • Salicylic Acid

  • Salsalate

  • Sodium Salicylate

  • Sodium Thiosalicylate

  • Trolamine Salicylate

Interactions with Food/Tobacco/Alcohol


Certain medicines should not be used at or around the time of eating food or eating certain types of food since interactions may occur. Using alcohol or tobacco with certain medicines may also cause interactions to occur. Discuss with your healthcare professional the use of your medicine with food, alcohol, or tobacco.


Other Medical Problems


The presence of other medical problems may affect the use of nadroparin. Make sure you tell your doctor if you have any other medical problems, especially:


  • Abortion (risk of) or

  • Bleeding problems or

  • Eye problems caused by diabetes or high blood pressure or

  • Heart infection or

  • High blood pressure or

  • Injury or surgery involving the brain, ears, eyes, or spinal cord or

  • Liver disease or

  • Low blood platelet count or

  • Stomach or intestinal ulcer or

  • Stroke—The risk of bleeding may be increased

  • Kidney disease—Nadroparin is removed from the body by the kidneys; patients with kidney disease may need to receive a lower dose of nadroparin

Proper Use of nadroparin


If you are using nadroparin at home, your health care professional will teach you how to inject yourself with the medicine. Be sure to follow the directions carefully. Check with your health care professional if you have any problems using the medicine.


Put used syringes in a puncture-resistant, disposable container or dispose of them as directed by your health care professional.


Dosing


The dose of nadroparin will be different for different patients. Follow your doctor's orders or the directions on the label. The following information includes only the average doses of nadroparin. If your dose is different, do not change it unless your doctor tells you to do so.


The amount of medicine that you take depends on the strength of the medicine. Also, the number of doses you take each day, the time allowed between doses, and the length of time you take the medicine depend on the medical problem for which you are using the medicine.


  • For injection dosage form:
    • For unstable angina or certain types of heart attacks:
      • Adults: The dose is based on body weight. It is usually 86 anti-factor Xa International Units (IU) per kilogram (kg) (39.1 anti-factor Xa IU per pound) of body weight injected under the skin every twelve hours for six days.

      • Children: Use and dose must be determined by your doctor.


    • For prevention of deep vein thrombosis (blood clots in the legs) or pulmonary embolism (blood clots in the lungs) after general surgery:
      • Adults: The dose is usually 2850 anti-factor Xa IU injected under the skin once a day beginning two to four hours before surgery and continuing for at least seven days.

      • Children: Use and dose must be determined by your doctor.


    • For prevention of deep vein thrombosis or pulmonary embolism after hip replacement surgery:
      • Adults: The dose is usually 38 anti-factor Xa IU per kg (17.3 anti-factor Xa IU per pound) of body weight injected under the skin twelve hours before surgery, twelve hours after surgery, and once a day for the first three days after surgery. Then, the dose is 57 anti-factor Xa IU per kg (26 anti-factor Xa IU per pound) of body weight injected under the skin once a day from the fourth through the tenth days after surgery.

      • Children: Use and dose must be determined by your doctor.


    • For treatment of deep vein thrombosis:
      • Adults:
        • Patients weighing less than 40 kg (88 pounds) or more than 100 kg (220 pounds): Dose must be determined by your doctor.

        • Patients weighing 40 to 100 kg (88 to 220 pounds): The dose is usually 171 anti-factor Xa IU per kg (77.7 anti-factor Xa IU per pound) of body weight injected under the skin once a day. Or, the dose may be 86 anti-factor Xa IU per kg (39.1 anti-factor Xa IU per pound) of body weight injected under the skin two times a day.


      • Children: Use and dose must be determined by your doctor.


    • For prevention of blood clots during hemodialysis (kidney dialysis):
      • Adults: The dose is usually 65 anti-factor Xa IU per kg (29.5 anti-factor Xa IU per pound) of body weight injected into an artery at the start of each dialysis session.

      • Children: Use and dose must be determined by your doctor.



Storage


Store the medicine in a closed container at room temperature, away from heat, moisture, and direct light. Keep from freezing.


Keep out of the reach of children.


Do not keep outdated medicine or medicine no longer needed.


Ask your healthcare professional how you should dispose of any medicine you do not use.


Precautions While Using nadroparin


Tell all of your medical doctors and dentists that you are using nadroparin.


nadroparin Side Effects


Along with its needed effects, a medicine may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention.


Stop taking nadroparin and get emergency help immediately if any of the following effects occur:


More common
  • Deep, dark purple bruise, pain, or swelling at place of injection

Rare
  • Back pain

  • black, tarry stools

  • bleeding from the mouth or gums

  • blood in the urine

  • blue-green to black skin discoloration

  • bluish discoloration, flushing, or redness of skin

  • burning, pricking, tickling, or tingling sensation

  • coughing

  • difficulty in swallowing

  • dizziness or feeling faint

  • fever

  • hives

  • itching

  • leg weakness

  • nosebleed

  • numbness

  • paralysis

  • problems with bladder or bowel function

  • redness or sloughing of skin at place of injection

  • skin rash

  • small purple or red spots in the mouth, on the gums, or on the skin

  • swelling of eyelids, face, or lips

  • tightness in chest, troubled breathing, and/or wheezing

  • vomiting of blood or coffee ground–like material

Other side effects not listed may also occur in some patients. If you notice any other effects, check with your healthcare professional.


Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088.



The information contained in the Thomson Reuters Micromedex products as delivered by Drugs.com is intended as an educational aid only. It is not intended as medical advice for individual conditions or treatment. It is not a substitute for a medical exam, nor does it replace the need for services provided by medical professionals. Talk to your doctor, nurse or pharmacist before taking any prescription or over the counter drugs (including any herbal medicines or supplements) or following any treatment or regimen. Only your doctor, nurse, or pharmacist can provide you with advice on what is safe and effective for you.


The use of the Thomson Reuters Healthcare products is at your sole risk. These products are provided "AS IS" and "as available" for use, without warranties of any kind, either express or implied. Thomson Reuters Healthcare and Drugs.com make no representation or warranty as to the accuracy, reliability, timeliness, usefulness or completeness of any of the information contained in the products. Additionally, THOMSON REUTERS HEALTHCARE MAKES NO REPRESENTATION OR WARRANTIES AS TO THE OPINIONS OR OTHER SERVICE OR DATA YOU MAY ACCESS, DOWNLOAD OR USE AS A RESULT OF USE OF THE THOMSON REUTERS HEALTHCARE PRODUCTS. ALL IMPLIED WARRANTIES OF MERCHANTABILITY AND FITNESS FOR A PARTICULAR PURPOSE OR USE ARE HEREBY EXCLUDED. Thomson Reuters Healthcare does not assume any responsibility or risk for your use of the Thomson Reuters Healthcare products.

Aténolol Actavis




Aténolol Actavis may be available in the countries listed below.


Ingredient matches for Aténolol Actavis



Atenolol

Atenolol is reported as an ingredient of Aténolol Actavis in the following countries:


  • France

International Drug Name Search

Calciprat




Calciprat may be available in the countries listed below.


Ingredient matches for Calciprat



Calcium Carbonate

Calcium Carbonate is reported as an ingredient of Calciprat in the following countries:


  • France

  • Tunisia

International Drug Name Search

Pamol Flash




Pamol Flash may be available in the countries listed below.


Ingredient matches for Pamol Flash



Paracetamol

Paracetamol is reported as an ingredient of Pamol Flash in the following countries:


  • Denmark

International Drug Name Search

International Apex Morphine




International Apex Morphine may be available in the countries listed below.


Ingredient matches for International Apex Morphine



Morphine

Morphine sulphate pentahydrate (a derivative of Morphine) is reported as an ingredient of International Apex Morphine in the following countries:


  • Philippines

International Drug Name Search

Monday, 26 September 2016

Cefamezin Alfa




Cefamezin Alfa may be available in the countries listed below.


Ingredient matches for Cefamezin Alfa



Cefazolin

Cefazolin sodium salt (a derivative of Cefazolin) is reported as an ingredient of Cefamezin Alfa in the following countries:


  • Japan

International Drug Name Search

Irapen




Irapen may be available in the countries listed below.


Ingredient matches for Irapen



Ampicillin

Ampicillin is reported as an ingredient of Irapen in the following countries:


  • Oman

International Drug Name Search

indometacine Apotex




indometacine Apotex may be available in the countries listed below.


Ingredient matches for indometacine Apotex



Indometacin

Indometacin is reported as an ingredient of indometacine Apotex in the following countries:


  • Netherlands

International Drug Name Search

Tramadol Extended-Release Tablets



Pronunciation: TRAM-a-dol
Generic Name: Tramadol
Brand Name: Examples include Ultram ER and Ryzolt


Tramadol Extended-Release Tablets are used for:

Treating moderate to moderately severe chronic pain in certain patients.


Tramadol Extended-Release Tablets are an analgesic. It works in certain areas of the brain and nervous system to decrease pain.


Do NOT use Tramadol Extended-Release Tablets if:


  • you are allergic to any ingredient in Tramadol Extended-Release Tablets

  • you have had a severe allergic reaction (rash; hives; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue) to codeine or another opioid (eg, morphine)

  • you have severe or persistent diarrhea due to taking an antibiotic

  • you have suicidal thoughts or actions or a history of alcohol or other substance abuse or addiction

  • you are intoxicated with alcohol, opioids or narcotics (eg, codeine, morphine), or sedatives or sleeping medicines (eg, temazepam, zolpidem)

  • you have severe liver or kidney problems

  • you are taking carbamazepine, nefazodone, sodium oxybate (GHB), a thioxanthene (eg, thiothixene), or another product that contains tramadol

Contact your doctor or health care provider right away if any of these apply to you.



Before using Tramadol Extended-Release Tablets:


Some medical conditions may interact with Tramadol Extended-Release Tablets. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:


  • if you are pregnant, planning to become pregnant, or are breast-feeding

  • if you are taking any prescription (especially depression medicines) or nonprescription medicine, herbal preparation, or dietary supplement

  • if you have allergies to medicines, foods, or other substances

  • if you have liver, kidney, or thyroid problems; a blockage in the bladder; diabetes; heart problems (eg, cor pulmonale); high blood pressure; pancreas problems; prostate problems; or metabolism problems

  • if you have or recently have had any head injury, brain injury or tumor, increased pressure in the brain, or infection of the brain or nervous system

  • if you have a history of recent stomach or bowel surgery, or any other stomach or bowel problems (eg, pain, inflammation, ulcers)

  • if you have a history of lung or breathing problems (eg, asthma, chronic obstructive pulmonary disease [COPD]) or seizures (eg, epilepsy)

  • if you drink alcohol; you are going through withdrawal from alcohol or other substances; or if you have a history of alcohol or other substance abuse or addiction, mood or mental problems (eg, depression), or suicidal thoughts or actions

Some MEDICINES MAY INTERACT with Tramadol Extended-Release Tablets. Tell your health care provider if you are taking any other medicines, especially any of the following:


  • Alpha-2 receptor blockers (eg, yohimbine), azole antifungals (eg, ketoconazole), linezolid, lithium, macrolide antibiotics (eg, erythromycin), monoamine oxidase inhibitors (MAOIs) (eg, phenelzine, selegiline), nefazodone, quinidine, selective serotonin reuptake inhibitors (SSRIs) (eg, fluoxetine, paroxetine), serotonin-norepinephrine reuptake inhibitors (SNRIs) (eg, duloxetine), St. John's wort, tricyclic antidepressants (eg, amitriptyline), or "triptans" (eg, sumatriptan) because serotonin syndrome may occur

  • Anorexiants (eg, phentermine), butyrophenones (eg, haloperidol), cyclobenzaprine, furazolidone, loxapine, certain medicines for mental or mood disorders (eg, olanzapine), molindone, opioid pain medicines (eg, codeine , hydrocodone), phenothiazines (eg, promethazine), sleeping medicines (eg, zolpidem); sodium oxybate (GHB), thioxanthenes (eg, thiothixene), or tiagabine because the risk of side effects, including excessive drowsiness, trouble breathing, liver problems, or seizures, may be increased

  • Carbamazepine because it may decrease Tramadol Extended-Release Tablets's effectiveness; the risk of seizures may also be increased

  • Other products containing tramadol because they may increase the risk of Tramadol Extended-Release Tablets's side effects

  • Rifampin because it may decrease Tramadol Extended-Release Tablets's effectiveness

  • Anticoagulants (eg, warfarin) or digoxin because the risk of their side effects may be increased by Tramadol Extended-Release Tablets

This may not be a complete list of all interactions that may occur. Ask your health care provider if Tramadol Extended-Release Tablets may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.


How to use Tramadol Extended-Release Tablets:


Use Tramadol Extended-Release Tablets as directed by your doctor. Check the label on the medicine for exact dosing instructions.


  • Take Tramadol Extended-Release Tablets by mouth with or without food. Try to take it the same way (either with food or without food) each time you take your dose. Check with your doctor or pharmacist if you have questions about taking Tramadol Extended-Release Tablets with food.

  • Swallow Tramadol Extended-Release Tablets whole. Do not break, crush, or chew before swallowing.

  • If you miss a dose of Tramadol Extended-Release Tablets and you are taking it regularly, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Tramadol Extended-Release Tablets.



Important safety information:


  • Tramadol Extended-Release Tablets may cause drowsiness, dizziness, or blurred vision. These effects may be worse if you take it with alcohol or certain medicines. Use Tramadol Extended-Release Tablets with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.

  • Do not drink alcohol while you are taking Tramadol Extended-Release Tablets.

  • Check with your doctor before you use medicines that may cause drowsiness (eg, sleep aids, muscle relaxers, narcotic pain medicines) while you are using Tramadol Extended-Release Tablets; it may add to their effects. Ask your pharmacist if you have questions about which medicines may cause drowsiness.

  • Tramadol Extended-Release Tablets may cause dizziness; alcohol, hot weather, exercise, or fever may increase this effect. To prevent it, sit up or stand slowly, especially in the morning. Sit or lie down at the first sign of this effect.

  • Do NOT take more than the recommended dose or take for longer than prescribed without checking with your doctor.

  • Tell your doctor or dentist that you take Tramadol Extended-Release Tablets before you receive any medical or dental care, emergency care, or surgery.

  • Tramadol Extended-Release Tablets may increase your risk of seizures. Your risk may be greater if you also have certain medical conditions, use certain medicines, or if you use a lot of alcohol. Talk to your doctor to see if you may have a greater risk of seizures while taking Tramadol Extended-Release Tablets.

  • Serotonin syndrome is a possibly fatal syndrome that can be caused by Tramadol Extended-Release Tablets. Your risk may be greater if you take Tramadol Extended-Release Tablets with certain other medicines (eg, "triptans," MAOIs, antidepressants). Symptoms may include agitation; confusion; hallucinations; coma; fever; fast or irregular heartbeat; tremor; excessive sweating; and nausea, vomiting, or diarrhea. Contact your doctor at once if you have any of these symptoms.

  • Use Tramadol Extended-Release Tablets with caution in the ELDERLY; they may be more sensitive to its effects, especially constipation, weakness or tiredness, severe light-headedness, and indigestion.

  • Tramadol Extended-Release Tablets should not be used in CHILDREN younger than 16 years; safety and effectiveness in these children have not been confirmed.

  • PREGNANCY and BREAST-FEEDING: Tramadol Extended-Release Tablets has been shown to cause harm to the fetus. If you think you may be pregnant, contact your doctor. You will need to discuss the benefits and risks of taking Tramadol Extended-Release Tablets while you are pregnant. Tramadol Extended-Release Tablets are found in breast milk. Do not breast-feed while taking Tramadol Extended-Release Tablets.

When used for long periods of time or at high doses, Tramadol Extended-Release Tablets may not work as well and may require higher doses to obtain the same effect as when originally taken. This is known as TOLERANCE. Talk with your doctor if Tramadol Extended-Release Tablets stops working well. Do not take more than prescribed.


Some people who use Tramadol Extended-Release Tablets for a long time without a break may develop a physical need to continue taking it. This is known as physical DEPENDENCE.


If you suddenly stop taking Tramadol Extended-Release Tablets, you may experience WITHDRAWAL symptoms, including anxiety; diarrhea; fever, runny nose, or sneezing; goose bumps and abnormal skin sensations; nausea; vomiting; pain; rigid muscles; rapid heartbeat; seeing, hearing or feeling things that are not there; shivering or tremors; sweating; and trouble sleeping. Do not suddenly stop taking Tramadol Extended-Release Tablets without talking with your doctor. If you need to stop Tramadol Extended-Release Tablets, your doctor will lower your dose over time.



Possible side effects of Tramadol Extended-Release Tablets:


All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:



Constipation; diarrhea; dizziness; drowsiness; dry mouth; headache; increased sweating; indigestion; mild itching; nausea; trouble sleeping; vomiting; weakness.



Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue; unusual hoarseness); agitation; chest pain; confusion; difficult or painful urination; disorientation; excessive sweating; fainting; fast or irregular heartbeat; fever; hallucinations; loss of coordination; mood or mental changes (eg, depression); red, blistered, swollen, or peeling skin; seizures; severe dizziness or light-headedness; severe nausea, vomiting, or diarrhea; severe or persistent headache; slow or shallow breathing; suicidal thoughts or behaviors; tremor; vision problems.



This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.


See also: Tramadol side effects (in more detail)


If OVERDOSE is suspected:


Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include bluish skin; cold, clammy skin; difficult, shallow, or slow breathing; drowsiness leading to unresponsiveness or coma; excessive sweating; limp muscles; pinpoint pupils; seizures; slow or irregular heartbeat.


Proper storage of Tramadol Extended-Release Tablets:

Store Tramadol Extended-Release Tablets at 77 degrees F (25 degrees C). Brief storage at temperatures between 59 and 86 degrees F (15 and 30 degrees C) is permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Tramadol Extended-Release Tablets out of the reach of children and away from pets.


General information:


  • If you have any questions about Tramadol Extended-Release Tablets, please talk with your doctor, pharmacist, or other health care provider.

  • Tramadol Extended-Release Tablets are to be used only by the patient for whom it is prescribed. Do not share it with other people.

  • If your symptoms do not improve or if they become worse, check with your doctor.

  • Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Tramadol Extended-Release Tablets. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.



Issue Date: February 1, 2012

Database Edition 12.1.1.002

Copyright © 2012 Wolters Kluwer Health, Inc.

More Tramadol resources


  • Tramadol Side Effects (in more detail)
  • Tramadol Dosage
  • Tramadol Use in Pregnancy & Breastfeeding
  • Drug Images
  • Tramadol Drug Interactions
  • Tramadol Support Group
  • 466 Reviews for Tramadol - Add your own review/rating


Compare Tramadol with other medications


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  • Vulvodynia

Ipsilon




Ipsilon may be available in the countries listed below.


Ingredient matches for Ipsilon



Aminocaproic Acid

Aminocaproic Acid is reported as an ingredient of Ipsilon in the following countries:


  • Argentina

  • Brazil

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Tipuric




Tipuric may be available in the countries listed below.


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Allopurinol

Allopurinol is reported as an ingredient of Tipuric in the following countries:


  • Ireland

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Pharmaseal Scrub Care




Ingredient matches for Pharmaseal Scrub Care



Chlorhexidine

Chlorhexidine digluconate (a derivative of Chlorhexidine) is reported as an ingredient of Pharmaseal Scrub Care in the following countries:


  • United States

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Heparin AL




Heparin AL may be available in the countries listed below.


Ingredient matches for Heparin AL



Heparin

Heparin sodium salt (a derivative of Heparin) is reported as an ingredient of Heparin AL in the following countries:


  • Czech Republic

  • Germany

  • Hungary

  • Slovakia

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Friday, 23 September 2016

Isoprenalina Cloridrato Monico




Isoprenalina Cloridrato Monico may be available in the countries listed below.


Ingredient matches for Isoprenalina Cloridrato Monico



Isoprenaline

Isoprenaline hydrochloride (a derivative of Isoprenaline) is reported as an ingredient of Isoprenalina Cloridrato Monico in the following countries:


  • Italy

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Insulina Insulatard HM




Insulina Insulatard HM may be available in the countries listed below.


Ingredient matches for Insulina Insulatard HM



Insulin, Isophane

Insulin, Isophane human (a derivative of Insulin, Isophane) is reported as an ingredient of Insulina Insulatard HM in the following countries:


  • Argentina

International Drug Name Search

Trinitrine Simple Laleuf




Trinitrine Simple Laleuf may be available in the countries listed below.


Ingredient matches for Trinitrine Simple Laleuf



Nitroglycerin

Nitroglycerin is reported as an ingredient of Trinitrine Simple Laleuf in the following countries:


  • France

  • Tunisia

International Drug Name Search

Flurablastin




Flurablastin may be available in the countries listed below.


Ingredient matches for Flurablastin



Fluorouracil

Fluorouracil is reported as an ingredient of Flurablastin in the following countries:


  • Denmark

  • Finland

  • Iceland

  • Norway

International Drug Name Search

Isoramycin




Isoramycin may be available in the countries listed below.


Ingredient matches for Isoramycin



Fosfomycin

Fosfomycin is reported as an ingredient of Isoramycin in the following countries:


  • Japan

International Drug Name Search

Norages




Norages may be available in the countries listed below.


Ingredient matches for Norages



Metamizole

Metamizole sodium anhydrous (a derivative of Metamizole) is reported as an ingredient of Norages in the following countries:


  • Indonesia

Norepinephrine

Norepinephrine tartrate (a derivative of Norepinephrine) is reported as an ingredient of Norages in the following countries:


  • Spain

International Drug Name Search

Panamax




In the US, Panamax is a member of the drug class miscellaneous analgesics and is used to treat Fever, Muscle Pain, Pain and Sciatica.

Ingredient matches for Panamax



Paracetamol

Paracetamol is reported as an ingredient of Panamax in the following countries:


  • Australia

  • Taiwan

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Isokin




Isokin may be available in the countries listed below.


Ingredient matches for Isokin



Isoniazid

Isoniazid is reported as an ingredient of Isokin in the following countries:


  • India

International Drug Name Search

Thursday, 22 September 2016

Biosetron




Biosetron may be available in the countries listed below.


Ingredient matches for Biosetron



Ondansetron

Ondansetron hydrochloride dihydrate (a derivative of Ondansetron) is reported as an ingredient of Biosetron in the following countries:


  • Greece

International Drug Name Search

Ipstyl Lyfjaver




Ipstyl Lyfjaver may be available in the countries listed below.


Ingredient matches for Ipstyl Lyfjaver



Lanreotide

Lanreotide is reported as an ingredient of Ipstyl Lyfjaver in the following countries:


  • Iceland

International Drug Name Search

Insuman Comb 25




Insuman Comb 25 may be available in the countries listed below.


Ingredient matches for Insuman Comb 25



Insulin Injection, Biphasic Isophane

Insulin Injection, Biphasic Isophane human (a derivative of Insulin Injection, Biphasic Isophane) is reported as an ingredient of Insuman Comb 25 in the following countries:


  • Austria

  • Bangladesh

  • Bosnia & Herzegowina

  • Bulgaria

  • Costa Rica

  • Czech Republic

  • Dominican Republic

  • El Salvador

  • Finland

  • France

  • Germany

  • Guatemala

  • Honduras

  • Ireland

  • Luxembourg

  • Netherlands

  • Nicaragua

  • Panama

  • Poland

  • Portugal

  • Romania

  • Russian Federation

  • Serbia

  • Slovakia

  • Sweden

  • Switzerland

  • United Kingdom

Insulin, Isophane

Insulin, Isophane human (a derivative of Insulin, Isophane) is reported as an ingredient of Insuman Comb 25 in the following countries:


  • Norway

International Drug Name Search

Alendronate Teva




Alendronate-Teva may be available in the countries listed below.


Ingredient matches for Alendronate-Teva



Alendronic Acid

Alendronic Acid is reported as an ingredient of Alendronate-Teva in the following countries:


  • France

  • Poland

Alendronic Acid sodium trihydrate (a derivative of Alendronic Acid) is reported as an ingredient of Alendronate-Teva in the following countries:


  • Belgium

  • Czech Republic

  • Israel

International Drug Name Search

Wednesday, 21 September 2016

Isopto-Dex




Isopto-Dex may be available in the countries listed below.


Ingredient matches for Isopto-Dex



Dexamethasone

Dexamethasone is reported as an ingredient of Isopto-Dex in the following countries:


  • Germany

International Drug Name Search

Teicoplanin Teva




Teicoplanin Teva may be available in the countries listed below.


Ingredient matches for Teicoplanin Teva



Teicoplanin

Teicoplanin is reported as an ingredient of Teicoplanin Teva in the following countries:


  • Switzerland

International Drug Name Search

Melus-Medichrom




Melus-Medichrom may be available in the countries listed below.


Ingredient matches for Melus-Medichrom



Meloxicam

Meloxicam is reported as an ingredient of Melus-Medichrom in the following countries:


  • Greece

International Drug Name Search

Daptomycin


Pronunciation: DAP-toe-MYE-sin
Generic Name: Daptomycin
Brand Name: Cubicin


Daptomycin is used for:

Treating serious infections caused by certain bacteria. It may also be used for other conditions as determined by your doctor.


Daptomycin is an antibiotic. It works by killing sensitive bacteria.


Do NOT use Daptomycin if:


  • you are allergic to any ingredient in Daptomycin

Contact your doctor or health care provider right away if any of these apply to you.



Before using Daptomycin:


Some medical conditions may interact with Daptomycin. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:


  • if you are pregnant, planning to become pregnant, or are breast-feeding

  • if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

  • if you have allergies to medicines, foods, or other substances

  • if you have muscle problems, nerve problems, liver problems, kidney problems, or bowel problems caused by antibiotic use

Some MEDICINES MAY INTERACT with Daptomycin. Tell your health care provider if you are taking any other medicines, especially any of the following:


  • HMG-CoA reductase inhibitors (eg, atorvastatin) or warfarin because the risk of their side effects may be increased by Daptomycin

  • Tobramycin because its effectiveness may be decreased by Daptomycin

This may not be a complete list of all interactions that may occur. Ask your health care provider if Daptomycin may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.


How to use Daptomycin:


Use Daptomycin as directed by your doctor. Check the label on the medicine for exact dosing instructions.


  • Daptomycin is usually given as an injection at your doctor's office, hospital, or clinic. If you will be using Daptomycin at home, a health care provider will teach you how to use it. Be sure you understand how to use Daptomycin. Follow the procedures you are taught when you use a dose. Contact your health care provider if you have any questions.

  • Do not use Daptomycin if it contains particles, is cloudy or discolored, or if the vial is cracked or damaged.

  • To clear up your infection completely, use Daptomycin for the full course of treatment. Keep using it even if you feel better in a few days.

  • Keep this product, as well as syringes and needles, out of the reach of children and pets. Do not reuse needles, syringes, or other materials. Ask your health care provider how to dispose of these materials after use. Follow all local rules for disposal.

  • If you miss a dose of Daptomycin, use it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not use 2 doses at once.

Ask your health care provider any questions you may have about how to use Daptomycin.



Important safety information:


  • Daptomycin may cause dizziness. This effect may be worse if you take it with alcohol or certain medicines. Use Daptomycin with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.

  • Daptomycin only works against bacteria; it does not treat viral infections (eg, the common cold).

  • Mild diarrhea is common with antibiotic use. However, a more serious form of diarrhea (pseudomembranous colitis) may rarely occur. This may develop while you use the antibiotic or within several months after you stop using it. Contact your doctor right away if stomach pain or cramps, severe diarrhea, or bloody stools occur. Do not treat diarrhea without first checking with your doctor.

  • Be sure to use Daptomycin for the full course of treatment. If you do not, the medicine may not clear up your infection completely. The bacteria could also become less sensitive to this or other medicines. This could make the infection harder to treat in the future.

  • Long-term or repeated use of Daptomycin may cause a second infection. Tell your doctor if signs of a second infection occur. Your medicine may need to be changed to treat this.

  • Eosinophilic pneumonia, a rare but serious condition, has been reported with the use of Daptomycin. Contact your doctor right away if you experience new or worsening fever, cough, shortness of breath, or trouble breathing. Discuss any questions or concerns with your doctor.

  • Lab tests, including white blood cell counts and creatine phosphokinase, may be performed while you use Daptomycin. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

  • Use Daptomycin with caution in the ELDERLY; they may be more sensitive to its effects.

  • Daptomycin should be used with extreme caution in CHILDREN younger than 18 years old; safety and effectiveness in these children have not been confirmed.

  • PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Daptomycin while you are pregnant. It is not known if Daptomycin is found in breast milk. If you are or will be breast-feeding while you use Daptomycin, check with your doctor. Discuss any possible risks to your baby.


Possible side effects of Daptomycin:


All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:



Constipation; diarrhea; dizziness; headache; nausea; pain, swelling, or redness at the injection site; sore throat; sweating; trouble sleeping; vomiting.



Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; chest pain; tightness in the chest; swelling of the mouth, face, lips, or tongue); bloody or watery stools; change in the amount of urine produced; fever; muscle pain or weakness; numbness or tingling; severe or persistent diarrhea; stomach cramps/pain; swelling (eg, of the hands, ankles, feet); symptoms of eosinophilic pneumonia (eg, new or worsening fever, cough, shortness of breath, or trouble breathing); unusual tiredness or weakness.



This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.


See also: Daptomycin side effects (in more detail)


If OVERDOSE is suspected:


Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately.


Proper storage of Daptomycin:

Daptomycin is usually handled and stored by a health care provider. If you are using Daptomycin at home, store Daptomycin as directed by your pharmacist or health care provider. Keep Daptomycin out of the reach of children and away from pets.


General information:


  • If you have any questions about Daptomycin, please talk with your doctor, pharmacist, or other health care provider.

  • Daptomycin is to be used only by the patient for whom it is prescribed. Do not share it with other people.

  • If your symptoms do not improve or if they become worse, check with your doctor.

  • Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Daptomycin. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.



Issue Date: February 1, 2012

Database Edition 12.1.1.002

Copyright © 2012 Wolters Kluwer Health, Inc.

More Daptomycin resources


  • Daptomycin Side Effects (in more detail)
  • Daptomycin Use in Pregnancy & Breastfeeding
  • Daptomycin Drug Interactions
  • Daptomycin Support Group
  • 0 Reviews for Daptomycin - Add your own review/rating


  • Daptomycin Professional Patient Advice (Wolters Kluwer)

  • Daptomycin Monograph (AHFS DI)

  • Cubicin Consumer Overview

  • Cubicin Prescribing Information (FDA)

  • daptomycin Intravenous Advanced Consumer (Micromedex) - Includes Dosage Information



Compare Daptomycin with other medications


  • Bacteremia
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  • Skin Infection

Torasemide Hexal




Torasemide Hexal may be available in the countries listed below.


Ingredient matches for Torasemide Hexal



Torasemide

Torasemide is reported as an ingredient of Torasemide Hexal in the following countries:


  • Italy

International Drug Name Search

Rose Bengal Sodium I 131




Rose Bengal Sodium I 131 may be available in the countries listed below.


Ingredient matches for Rose Bengal Sodium I 131



Rose Bengal (131I) Sodium

Rose Bengal Sodium I 131 (USAN) is also known as Rose Bengal (131I) Sodium (Rec.INN)

International Drug Name Search

Glossary

Rec.INNRecommended International Nonproprietary Name (World Health Organization)
USANUnited States Adopted Name

Click for further information on drug naming conventions and International Nonproprietary Names.

Tuesday, 20 September 2016

Fertomid




Fertomid may be available in the countries listed below.


Ingredient matches for Fertomid



Clomifene

Clomifene citrate (a derivative of Clomifene) is reported as an ingredient of Fertomid in the following countries:


  • India

  • South Africa

International Drug Name Search

Noradrenaline Harvest Pharm




Noradrenaline Harvest Pharm may be available in the countries listed below.


Ingredient matches for Noradrenaline Harvest Pharm



Norepinephrine

Norepinephrine tartrate (a derivative of Norepinephrine) is reported as an ingredient of Noradrenaline Harvest Pharm in the following countries:


  • China

International Drug Name Search

Isoproterenol Hydrochloride




Ingredient matches for Isoproterenol Hydrochloride



Isoprenaline

Isoprenaline hydrochloride (a derivative of Isoprenaline) is reported as an ingredient of Isoproterenol Hydrochloride in the following countries:


  • United States

International Drug Name Search

Oprazol Spirig




Oprazol Spirig may be available in the countries listed below.


Ingredient matches for Oprazol Spirig



Omeprazole

Omeprazole is reported as an ingredient of Oprazol Spirig in the following countries:


  • Switzerland

International Drug Name Search

Ceroneed




Ceroneed may be available in the countries listed below.


Ingredient matches for Ceroneed



Ceftriaxone

Ceftriaxone disodium salt (a derivative of Ceftriaxone) is reported as an ingredient of Ceroneed in the following countries:


  • Japan

International Drug Name Search

Phloroglucinol G Gam




Phloroglucinol G Gam may be available in the countries listed below.


Ingredient matches for Phloroglucinol G Gam



Phloroglucinol

Phloroglucinol is reported as an ingredient of Phloroglucinol G Gam in the following countries:


  • France

International Drug Name Search

Interferone gamma




Interferone gamma may be available in the countries listed below.


Ingredient matches for Interferone gamma



Interferon gamma

Interferone gamma (DCIT) is also known as Interferon gamma (Rec.INN)

International Drug Name Search

Glossary

DCITDenominazione Comune Italiana
Rec.INNRecommended International Nonproprietary Name (World Health Organization)

Click for further information on drug naming conventions and International Nonproprietary Names.

Rozicel




Rozicel may be available in the countries listed below.


Ingredient matches for Rozicel



Cefprozil

Cefprozil monohydrate (a derivative of Cefprozil) is reported as an ingredient of Rozicel in the following countries:


  • Italy

International Drug Name Search

TBZ




In some countries, this medicine may only be approved for veterinary use.

Ingredient matches for TBZ



Tiabendazole

Tiabendazole is reported as an ingredient of TBZ in the following countries:


  • United States

International Drug Name Search

Cefzil


Generic Name: cefprozil (Oral route)

sef-PROE-zil

Commonly used brand name(s)

In the U.S.


  • Cefzil

Available Dosage Forms:


  • Tablet

  • Powder for Suspension

Therapeutic Class: Antibiotic


Pharmacologic Class: 2nd Generation Cephalosporin


Uses For Cefzil


Cefprozil is used to treat bacterial infections in many different parts of the body. It belongs to the class of medicines known as cephalosporin antibiotics. It works by killing bacteria or preventing their growth. However, this medicine will not work for colds, flu, or other virus infections.


This medicine is available only with your doctor's prescription.


Before Using Cefzil


In deciding to use a medicine, the risks of taking the medicine must be weighed against the good it will do. This is a decision you and your doctor will make. For this medicine, the following should be considered:


Allergies


Tell your doctor if you have ever had any unusual or allergic reaction to this medicine or any other medicines. Also tell your health care professional if you have any other types of allergies, such as to foods, dyes, preservatives, or animals. For non-prescription products, read the label or package ingredients carefully.


Pediatric


Appropriate studies performed to date have not demonstrated pediatric-specific problems that would limit the usefulness of cefprozil for otitis media (ear infection) and sinusitis in children 6 months to 12 years of age. However, safety and efficacy have not been established in infants younger than 6 months of age.


Appropriate studies performed to date have not demonstrated pediatric-specific problems that would limit the usefulness of cefprozil for sore throat and skin infections in children 2 to 12 years of age. However, safety and efficacy have not been established in children younger than 2 years of age.


Because of cefprozil's toxicity, use in newborn babies is not recommended.


Geriatric


Appropriate studies performed to date have not demonstrated geriatric-specific problems that would limit the usefulness of cefprozil in the elderly. However, elderly patients are more likely to have age-related kidney problems, which may require caution and an adjustment in the dose for patients receiving cefprozil.


Pregnancy








Pregnancy CategoryExplanation
All TrimestersBAnimal studies have revealed no evidence of harm to the fetus, however, there are no adequate studies in pregnant women OR animal studies have shown an adverse effect, but adequate studies in pregnant women have failed to demonstrate a risk to the fetus.

Breast Feeding


Studies in women suggest that this medication poses minimal risk to the infant when used during breastfeeding.


Interactions with Medicines


Although certain medicines should not be used together at all, in other cases two different medicines may be used together even if an interaction might occur. In these cases, your doctor may want to change the dose, or other precautions may be necessary. When you are taking this medicine, it is especially important that your healthcare professional know if you are taking any of the medicines listed below. The following interactions have been selected on the basis of their potential significance and are not necessarily all-inclusive.


Using this medicine with any of the following medicines may cause an increased risk of certain side effects, but using both drugs may be the best treatment for you. If both medicines are prescribed together, your doctor may change the dose or how often you use one or both of the medicines.


  • Probenecid

Interactions with Food/Tobacco/Alcohol


Certain medicines should not be used at or around the time of eating food or eating certain types of food since interactions may occur. Using alcohol or tobacco with certain medicines may also cause interactions to occur. Discuss with your healthcare professional the use of your medicine with food, alcohol, or tobacco.


Other Medical Problems


The presence of other medical problems may affect the use of this medicine. Make sure you tell your doctor if you have any other medical problems, especially:


  • Colitis (inflammation in gut), history of or

  • Diarrhea, severe, history of—Use with caution. May make these conditions worse.

  • Kidney disease—Use with caution. Effects may be increased because of slower removal of the medicine from the body.

  • Phenylketonuria (PKU)—The oral liquid form of this medicine contains phenylalanine, which can make this condition worse.

Proper Use of Cefzil


Take this medicine only as directed by your doctor. Do not take more of it, do not take it more often, and do not take it for a longer time than your doctor ordered.


Shake the oral liquid well before each use. Measure the medicine with a marked measuring spoon, oral syringe, or medicine cup. The average household teaspoon may not hold the right amount of liquid.


Keep using this medicine for the full treatment time, even if you feel better after the first few doses. Your infection may not clear up if you stop using the medicine too soon.


Dosing


The dose of this medicine will be different for different patients. Follow your doctor's orders or the directions on the label. The following information includes only the average doses of this medicine. If your dose is different, do not change it unless your doctor tells you to do so.


The amount of medicine that you take depends on the strength of the medicine. Also, the number of doses you take each day, the time allowed between doses, and the length of time you take the medicine depend on the medical problem for which you are using the medicine.


  • For oral dosage forms (tablets or suspension):
    • For bronchitis:
      • Adults and teenagers—500 milligrams (mg) every 12 hours, taken for 10 days.

      • Children younger than 13 years of age—Use and dose must be determined by your doctor.


    • For ear infections:
      • Children 6 months to 12 years of age—Dose is based on body weight and must be determined by your doctor. The dose is usually 15 milligrams (mg) per kilogram (kg) of body weight every 12 hours, taken for 10 days.

      • Infants younger than 6 months of age—Use and dose must be determined by your doctor.


    • For sinusitis:
      • Adults and teenagers—250 or 500 milligrams (mg) every 12 hours for 10 days.

      • Children 6 months to 12 years of age—Dose is based on body weight and must be determined by your doctor. The dose is usually 7.5 to 15 milligrams (mg) per kilogram (kg) of body weight every 12 hours, taken for 10 days.

      • Infants younger than 6 months of age—Use and dose must be determined by your doctor.


    • For skin infections:
      • Adults and teenagers—250 to 500 milligrams (mg) every 12 hours or 500 mg once a day, taken for 10 days.

      • Children 2 to 12 years of age—Dose is based on body weight and must be determined by your doctor. The dose is usually 20 milligrams (mg) per kilogram (kg) of body weight per day, taken for 10 days.

      • Children younger than 2 years of age—Use and dose must be determined by your doctor.


    • For sore throat and tonsillitis:
      • Adults and teenagers—500 milligrams (mg) once a day for 10 days.

      • Children 2 to 12 years of age—Dose is based on body weight and must be determined by your doctor. The dose is usually 7.5 milligrams (mg) per kilogram (kg) of body weight every 12 hours, taken for 10 days.

      • Children younger than 2 years of age—Use and dose must be determined by your doctor.



Missed Dose


If you miss a dose of this medicine, take it as soon as possible. However, if it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not double doses.


Storage


Keep out of the reach of children.


Do not keep outdated medicine or medicine no longer needed.


Ask your healthcare professional how you should dispose of any medicine you do not use.


Store the oral liquid in the refrigerator. Throw away any unused medicine after 14 days.


Store the tablets in a closed container at room temperature, away from heat, moisture, and direct light. Keep from freezing.


Precautions While Using Cefzil


If your symptoms do not improve within a few days, or if they become worse, check with your doctor.


Cefprozil may cause diarrhea, and in some cases it can be severe. Do not take any medicine or give medicine to your child to treat diarrhea without first checking with your doctor. Diarrhea medicines may make the diarrhea worse or make it last longer. If you have any questions about this or if mild diarrhea continues or gets worse, check with your doctor.


Before you or your child have any medical tests, tell the medical doctor in charge that you are using this medicine. The results of some tests may be affected by this medicine.


Cefzil Side Effects


Along with its needed effects, a medicine may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention.


Check with your doctor immediately if any of the following side effects occur:


Less common
  • Black, tarry stools

  • chest pain

  • cough or hoarseness

  • diarrhea

  • fever or chills

  • lower back or side pain

  • painful or difficult urination

  • shortness of breath

  • sore throat sores, ulcers, or white spots on the lips or in the mouth

  • swollen glands

  • unusual bleeding or bruising

  • unusual tiredness or weakness

Rare
  • Abdominal or stomach cramps, pain, or tenderness

  • bleeding gums

  • blistering, peeling, or loosening of the skin

  • bloating

  • blood in the urine or stools

  • clay-colored stools

  • dark urine

  • diarrhea, watery and severe, which may also be bloody

  • difficulty with swallowing

  • dizziness

  • fast heartbeat

  • feeling of discomfort

  • headache

  • hives

  • increased thirst

  • inflammation of the joints

  • itching

  • joint or muscle pain

  • large, hive-like swelling on the face, eyelids, lips, tongue, throat, hands, legs, feet, or sex organs

  • loss of appetite

  • muscle aches

  • nausea or vomiting

  • pain

  • pinpoint red spots on the skin

  • puffiness or swelling of the eyelids or around the eyes, face, lips, or tongue

  • rash

  • red skin lesions, often with a purple center

  • red, irritated eyes

  • shortness of breath

  • swollen lymph glands

  • tightness in the chest

  • unpleasant breath odor

  • unusual weight loss

  • vomiting of blood

  • watery or bloody diarrhea

  • wheezing

  • yellow eyes or skin

Incidence not known
  • Back, leg, or stomach pains

  • bleeding gums

  • bloody or cloudy urine

  • bloody, black, or tarry stools

  • decrease in urine output or decrease in urine-concentrating ability

  • difficulty with breathing

  • fever with or without chills

  • general body swelling

  • general feeling of tiredness or weakness

  • high fever

  • nosebleeds

  • pale skin

  • sudden decrease in the amount of urine

  • swollen or painful glands

Some side effects may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects. Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them:


Less common
  • Itching or pain of the vagina or genital area

  • pain during sexual intercourse

  • thick, white vaginal discharge with no odor or with a mild odor

Rare
  • Confusion

  • hives or welts

  • nervousness

  • redness of the skin

  • restlessness

  • sleepiness or unusual drowsiness

  • sleeplessness

  • trouble sitting still

  • trouble with sleeping

  • unable to sleep

Other side effects not listed may also occur in some patients. If you notice any other effects, check with your healthcare professional.


Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088.

See also: Cefzil side effects (in more detail)



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More Cefzil resources


  • Cefzil Side Effects (in more detail)
  • Cefzil Use in Pregnancy & Breastfeeding
  • Drug Images
  • Cefzil Drug Interactions
  • Cefzil Support Group
  • 6 Reviews for Cefzil - Add your own review/rating


  • Cefzil Prescribing Information (FDA)

  • Cefzil Consumer Overview

  • Cefzil Monograph (AHFS DI)

  • Cefzil MedFacts Consumer Leaflet (Wolters Kluwer)

  • Cefprozil Prescribing Information (FDA)

  • Cefprozil Professional Patient Advice (Wolters Kluwer)



Compare Cefzil with other medications


  • Bladder Infection
  • Bronchitis
  • Kidney Infections
  • Otitis Media
  • Pneumonia
  • Sinusitis
  • Skin Infection
  • Tonsillitis/Pharyngitis
  • Upper Respiratory Tract Infection