Milador may be available in the countries listed below.
Tramadol hydrochloride (a derivative of Tramadol) is reported as an ingredient of Milador in the following countries:
International Drug Name Search
Treating mild to moderate dementia (eg, impairment of memory or judgement, abstract thinking, changes in personality) in patients with Alzheimer disease.
Razadyne Solution is a cholinesterase inhibitor. It works by increasing the amount of a certain substance (acetylcholine) in the brain, which may help reduce symptoms of dementia in patients with Alzheimer disease.
Contact your doctor or health care provider right away if any of these apply to you.
Some medical conditions may interact with Razadyne Solution. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:
Some MEDICINES MAY INTERACT with Razadyne Solution. Tell your health care provider if you are taking any other medicines, especially any of the following:
This may not be a complete list of all interactions that may occur. Ask your health care provider if Razadyne Solution 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.
Use Razadyne Solution as directed by your doctor. Check the label on the medicine for exact dosing instructions.
Ask your health care provider any questions you may have about how to use Razadyne Solution.
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:
Diarrhea; dizziness; headache; loss of appetite; nausea; stomach upset; tiredness; vomiting; weight loss.
Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); bloody, black, or tarry stools; chest pain; decreased urination; depression; fainting; fever; seizures; severe or persistent tiredness or weakness; slow or irregular heartbeat; tremor.
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: Razadyne side effects (in more detail)
Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include fainting; increased sweating or saliva production; loss of bowel control; loss of consciousness; muscle weakness; seizures; severe dizziness; severe nausea or vomiting; slow heartbeat; slow or shallow breathing; stomach cramping.
Store Razadyne Solution at 77 degrees F (25 degrees C). Brief storage at temperatures between 59 and 86 degrees F (15 and 30 degrees C) is permitted. Do NOT freeze. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Razadyne Solution out of the reach of children and away from pets.
This information is a summary only. It does not contain all information about Razadyne Solution. 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.
Daunorrubicina may be available in the countries listed below.
Daunorubicin hydrochloride (a derivative of Daunorubicin) is reported as an ingredient of Daunorrubicina in the following countries:
International Drug Name Search
Citaxin may be available in the countries listed below.
Citalopram hydrobromide (a derivative of Citalopram) is reported as an ingredient of Citaxin in the following countries:
International Drug Name Search
Treating opioid dependence. It should be used as part of a complete narcotic dependence treatment plan. It may also be used for other conditions as determined by your doctor.
Buprenorphine is an opioid (narcotic) partial agonist-antagonist. It works by binding to receptors in the brain and nervous system to help prevent withdrawal symptoms in someone who has stopped taking narcotics (eg, heroin, oxycodone).
Contact your doctor or health care provider right away if any of these apply to you.
Some medical conditions may interact with Buprenorphine. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:
Some MEDICINES MAY INTERACT with Buprenorphine. Tell your health care provider if you are taking any other medicines, especially any of the following:
This may not be a complete list of all interactions that may occur. Ask your health care provider if Buprenorphine 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.
Use Buprenorphine as directed by your doctor. Check the label on the medicine for exact dosing instructions.
Ask your health care provider any questions you may have about how to use Buprenorphine.
When used for long periods of time or at high doses, some people develop a need to continue taking Buprenorphine. This is known as DEPENDENCE or addiction.
If you suddenly stop taking Buprenorphine, 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.
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:
Chills; constipation; diarrhea; dizziness; drowsiness; flushing; headache; nausea; sleeplessness; stomach pain; sweating; vomiting; weakness.
Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); anxiety or nervousness; dark urine; mental or mood changes (eg, depression); pale stools; slow or shallow breathing; severe or persistent stomach pain; yellowing of eyes or skin.
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: Buprenorphine side effects (in more detail)
Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include excessive drowsiness; severe dizziness; very slow and shallow breathing; very small pupils.
Store Buprenorphine 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 Buprenorphine out of the reach of children and away from pets.
This information is a summary only. It does not contain all information about Buprenorphine. 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.
Tilidine Hydrochloride may be available in the countries listed below.
Tilidine Hydrochloride (USAN) is also known as Tilidine (Prop.INN)
International Drug Name Search
Glossary
| Prop.INN | Proposed International Nonproprietary Name (World Health Organization) |
| USAN | United States Adopted Name |
The following drugs and medications are in some way related to, or used in the treatment of SAPHO Syndrome. This service should be used as a supplement to, and NOT a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners.
Clorana may be available in the countries listed below.
Hydrochlorothiazide is reported as an ingredient of Clorana in the following countries:
International Drug Name Search
Treating or preventing low potassium blood levels when the amount of potassium in the diet is inadequate. Low potassium levels may also be caused by some diseases, severe or prolonged vomiting or diarrhea, or certain medicines (eg, diuretics). Symptoms of low potassium levels include weakness, fatigue, or weakening of reflexes.
Rum-K Liquid is an electrolyte that is needed for normal functioning of cells, nerve conduction, muscle contraction, kidney function, and acid-base balance.
Contact your doctor or health care provider right away if any of these apply to you.
Some medical conditions may interact with Rum-K Liquid. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:
Some MEDICINES MAY INTERACT with Rum-K Liquid. Tell your health care provider if you are taking any other medicines, especially any of the following:
This may not be a complete list of all interactions that may occur. Ask your health care provider if Rum-K Liquid 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.
Use Rum-K Liquid as directed by your doctor. Check the label on the medicine for exact dosing instructions.
Ask your health care provider any questions you may have about how to use Rum-K Liquid.
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 skin sensation; confusion; diarrhea; listlessness; nausea; stomach discomfort; vomiting.
Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); abnormal heartbeat; black, tarry stools; chest pain; heaviness in the legs; indigestion; irregular heartbeat; severe vomiting; stomach pain; tingling in the hands and feet; unusual tiredness or weakness; vomit that looks like coffee grounds.
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: Rum-K side effects (in more detail)
Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include chest pain; fast, slow, or irregular heartbeat; limp muscles; listlessness; muscle weakness or paralysis; slow or difficult breathing.
Store Rum-K Liquid at room temperature, between 59 and 86 degrees F (15 and 30 degrees C), in a tightly-closed container. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Rum-K Liquid out of the reach of children and away from pets.
This information is a summary only. It does not contain all information about Rum-K Liquid. 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.
Relieving cough and throat and airway irritation due to colds, flu, or hay fever. It may also be used for other conditions as determined by your doctor.
Hydrocodone/Potassium Guaiacolsulfonate Liquid is a cough suppressant and expectorant combination. It works by loosening mucus and lung secretions in the chest, and making coughs more productive. The cough suppressant works in the brain to help decrease the cough reflex to reduce a dry cough.
Contact your doctor or health care provider right away if any of these apply to you.
Some medical conditions may interact with Hydrocodone/Potassium Guaiacolsulfonate Liquid. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:
Some MEDICINES MAY INTERACT with Hydrocodone/Potassium Guaiacolsulfonate Liquid. Tell your health care provider if you are taking any other medicines, especially any of the following:
This may not be a complete list of all interactions that may occur. Ask your health care provider if Hydrocodone/Potassium Guaiacolsulfonate Liquid 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.
Use Hydrocodone/Potassium Guaiacolsulfonate Liquid as directed by your doctor. Check the label on the medicine for exact dosing instructions.
Ask your health care provider any questions you may have about how to use Hydrocodone/Potassium Guaiacolsulfonate Liquid.
When used for long periods of time or at high doses, Hydrocodone/Potassium Guaiacolsulfonate Liquid 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 Hydrocodone/Potassium Guaiacolsulfonate Liquid stops working well. Do not take more than prescribed.
When used for longer than a few weeks or at high doses, some people develop a need to continue taking Hydrocodone/Potassium Guaiacolsulfonate Liquid. This is known as DEPENDENCE or addiction.
If you suddenly stop taking Hydrocodone/Potassium Guaiacolsulfonate Liquid, 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.
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; dizziness; drowsiness; excitability; headache; nausea; nervousness or anxiety; trouble sleeping; weakness.
Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); anxiety; change in amount of urine; difficulty urinating; hearing change or loss; mental or mood changes; severe drowsiness.
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: Hydrocodone/Potassium Guaiacolsulfonate side effects (in more detail)
Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include blurred vision; confusion; hallucinations; seizures; severe dizziness, lightheadedness, or headache; severe drowsiness; unusually fast, slow, or irregular heartbeat; vomiting.
Store Hydrocodone/Potassium Guaiacolsulfonate Liquid at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Hydrocodone/Potassium Guaiacolsulfonate Liquid out of the reach of children and away from pets.
This information is a summary only. It does not contain all information about Hydrocodone/Potassium Guaiacolsulfonate Liquid. 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.
Betalan may be available in the countries listed below.
Betahistine dihydrochloride (a derivative of Betahistine) is reported as an ingredient of Betalan in the following countries:
International Drug Name Search
Cirumimeru may be available in the countries listed below.
Mexiletine hydrochloride (a derivative of Mexiletine) is reported as an ingredient of Cirumimeru in the following countries:
International Drug Name Search
Aeropax may be available in the countries listed below.
Dimeticone is reported as an ingredient of Aeropax in the following countries:
Simeticone is reported as an ingredient of Aeropax in the following countries:
International Drug Name Search
Clonapam may be available in the countries listed below.
Clonazepam is reported as an ingredient of Clonapam in the following countries:
International Drug Name Search
Etiprazol may be available in the countries listed below.
Omeprazole is reported as an ingredient of Etiprazol in the following countries:
International Drug Name Search
Statinal may be available in the countries listed below.
Simvastatin is reported as an ingredient of Statinal in the following countries:
International Drug Name Search
Generic Name: potassium citrate (Oral route)
poe-TAS-ee-um SIT-rate
In the U.S.
Available Dosage Forms:
Therapeutic Class: Urinary Alkalinizer
Potassium citrate is used to treat a kidney stone condition called renal tubular acidosis. It is also used to prevent kidney stones that may occur with gout.
Potassium citrate is a urinary alkalinizer. It works by making the urine more alkaline (less acid).
This medicine is available only with your doctor's prescription.
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:
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.
Appropriate studies have not been performed on the relationship of age to the effects of potassium citrate in the pediatric population. Safety and efficacy have not been established.
No information is available on the relationship of age to the effects of potassium citrate in geriatric patients.
| Pregnancy Category | Explanation | |
|---|---|---|
| All Trimesters | C | Animal studies have shown an adverse effect and there are no adequate studies in pregnant women OR no animal studies have been conducted and there are no adequate studies in pregnant women. |
There are no adequate studies in women for determining infant risk when using this medication during breastfeeding. Weigh the potential benefits against the potential risks before taking this medication while breastfeeding.
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. Tell your healthcare professional if you are taking any other prescription or nonprescription (over-the-counter [OTC]) medicine.
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.
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:
This section provides information on the proper use of a number of products that contain potassium citrate. It may not be specific to Urocit-K 15. Please read with care.
Take this medicine exactly 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. To do so may increase the chance of side effects.
In addition to the use of this medicine, treatment for your kidney stones may include changes in the types of foods you eat, especially foods high in sodium (salt). Your doctor will tell you which of these are most important for you. You should check with your doctor before changing your diet.
It is best to take this medicine with a meal or bedtime snack, or within 30 minutes after meals.
Swallow the extended-release tablet whole. Do not break, crush, chew, or suck it. Doing so, may cause irritation in the mouth or throat.
Tell your doctor if you have trouble swallowing the tablets, or if the tablet seems to stick or gets stuck in your throat.
While taking the extended-release tablet, part of it may pass into your stools. This is normal and is nothing to worry about.
Drink extra fluids so you will pass more urine while you are using this medicine. This will keep your kidneys working well and help prevent kidney problems.
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.
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.
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.
It is very important that your doctor check your progress at regular visits to make sure that this medicine is working properly. Blood and urine tests may be needed to check for unwanted effects.
You should not take this medicine if you are also using atropine, benztropine (Cogentin®), glycopyrrolate (Robinul®), or a diuretic or "water pill" (such as amiloride, spironolactone, triamterene, Aldactone®, Dyrenium®, or Midamor®). Using these medicines together may cause serious problems.
Hyperkalemia (high potassium in the blood) may occur while you are using this medicine. Stop using this medicine and check with your doctor right away if you have the following symptoms: abdominal or stomach pain; confusion; difficulty with breathing; irregular heartbeat; nausea or vomiting; nervousness; numbness or tingling in the hands, feet, or lips; shortness of breath; or weakness or heaviness of the legs.
Stop using this medicine and check with your doctor right away if you have bloody or black, tarry stools; constipation; severe stomach pain; or vomiting of blood or material that looks like coffee grounds. These may be symptoms of a serious stomach problem.
Do not take other medicines unless they have been discussed with your doctor. This includes prescription or nonprescription (over-the-counter [OTC]) medicines and herbal or vitamin supplements.
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:
Get emergency help immediately if any of the following symptoms of overdose occur:
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: Urocit-K5 Oral side effects (in more detail)
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.
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Ciprofloxacino Ur may be available in the countries listed below.
Ciprofloxacin hydrochloride (a derivative of Ciprofloxacin) is reported as an ingredient of Ciprofloxacino Ur in the following countries:
International Drug Name Search
Gluco-Rite may be available in the countries listed below.
Glipizide is reported as an ingredient of Gluco-Rite in the following countries:
International Drug Name Search
Fenazil may be available in the countries listed below.
Promethazine hydrochloride (a derivative of Promethazine) is reported as an ingredient of Fenazil in the following countries:
International Drug Name Search
Alantan-Plus may be available in the countries listed below.
Allantoin is reported as an ingredient of Alantan-Plus in the following countries:
Dexpanthenol is reported as an ingredient of Alantan-Plus in the following countries:
International Drug Name Search
Tenicef may be available in the countries listed below.
Ceftazidime pentahydrate (a derivative of Ceftazidime) is reported as an ingredient of Tenicef in the following countries:
International Drug Name Search
Ciprofloxacinum may be available in the countries listed below.
Ciprofloxacin is reported as an ingredient of Ciprofloxacinum in the following countries:
International Drug Name Search
Pamacid may be available in the countries listed below.
Famotidine is reported as an ingredient of Pamacid in the following countries:
International Drug Name Search
Generic Name: chlorhexidine topical (klor HEX i deen TOP i kal)
Brand Names: Betasept, Biopatch, Calgon Vesta, Chlorostat, Chlorostat 4, Dyna-Hex, Hibiclens, PerioChip, Spectrum-4
Chlorhexidine is an antiseptic that fights bacteria.
Chlorhexidine topical (for the skin) is used to clean the skin to prevent infection that may be caused by surgery, injection, or skin injury.
Chlorhexidine topical may also be used for purposes not listed in this medication guide.
Ask a doctor or pharmacist if it is safe for you to use chlorhexidine topical if you have any allergies to food, dyes, animals, or medicines.
Stop using the medication and call your doctor if you have a skin reaction such as severe burning, itching, redness, blistering, peeling, swelling, rash, or any other severe irritation.
Ask a doctor or pharmacist if it is safe for you to use this medicine if you have any allergies to food, dyes, animals, or medicines.
Use exactly as directed on the label, or as prescribed by your doctor. Do not use in larger or smaller amounts or for longer than recommended.
Rinse the skin before applying chlorhexidine topical gel or dressing. Apply only enough to cover the area you are treating.
To use chlorhexidine topical soap, apply only enough to cover the area you are treating. Wash the area gently, then rinse thoroughly with plain water. Avoid using over large areas of skin.
Call your doctor if your symptoms do not improve, or if they get worse while using chlorhexidine topical.
Use the missed dose as soon as you remember. Skip the missed dose if it is almost time for your next scheduled dose. Do not use extra medicine to make up the missed dose.
Avoid using other medications on the areas you treat with chlorhexidine topical unless you doctor tells you to.
Avoid getting this medication on your clothing or other fabrics. Do not use bleach to wash any fabric exposed to chlorhexidine or the medicine may cause a permanent stain.
severe burning, itching, or redness;
blistering or peeling;
swelling or severe skin rash; or
any other severe irritation of treated skin.
Less serious side effects may occur, and you may have none at all.
This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.
It is not likely that other drugs you take orally or inject will have an effect on topically applied chlorhexidine topical. But many drugs can interact with each other. Tell your doctor about all medications you use. This includes prescription, over-the-counter, vitamin, and herbal products. Do not start a new medication without telling your doctor.
See also: Hibistat side effects (in more detail)
Coronovo may be available in the countries listed below.
Amiodarone hydrochloride (a derivative of Amiodarone) is reported as an ingredient of Coronovo in the following countries:
International Drug Name Search
Lévonorgestrel may be available in the countries listed below.
Lévonorgestrel (DCF) is known as Levonorgestrel in the US.
International Drug Name Search
Glossary
| DCF | Dénomination Commune Française |
Plitican may be available in the countries listed below.
Alizapride hydrochloride (a derivative of Alizapride) is reported as an ingredient of Plitican in the following countries:
International Drug Name Search
Cipromid may be available in the countries listed below.
Ciprofloxacin hydrochloride (a derivative of Ciprofloxacin) is reported as an ingredient of Cipromid in the following countries:
International Drug Name Search
Ciprofloxacino Winthrop may be available in the countries listed below.
Ciprofloxacin hydrochloride (a derivative of Ciprofloxacin) is reported as an ingredient of Ciprofloxacino Winthrop in the following countries:
International Drug Name Search
In the US, Avastin (bevacizumab systemic) is a member of the drug class VEGF/VEGFR inhibitors and is used to treat Breast Cancer, Breast Cancer - Metastatic, Colorectal Cancer, Glioblastoma Multiforme, Macular Degeneration, Malignant Glioma, Neurofibromatosis, Non-Small Cell Lung Cancer, Ovarian Cancer, Pancreatic Cancer, Renal Cell Carcinoma and Solid Tumors.
US matches:
UK matches:
Bevacizumab is reported as an ingredient of Avastin in the following countries:
Simvastatin is reported as an ingredient of Avastin in the following countries:
International Drug Name Search
Glossary
| SPC | Summary of Product Characteristics (UK) |
Kitasamycin Tartrate may be available in the countries listed below.
Kitasamycin Tartrate (JAN) is also known as Kitasamycin (Rec.INN)
International Drug Name Search
Glossary
| JAN | Japanese Accepted Name |
| Rec.INN | Recommended International Nonproprietary Name (World Health Organization) |
Nilaflox may be available in the countries listed below.
Ciprofloxacin is reported as an ingredient of Nilaflox in the following countries:
International Drug Name Search
Venlasan may be available in the countries listed below.
Venlafaxine hydrochloride (a derivative of Venlafaxine) is reported as an ingredient of Venlasan in the following countries:
International Drug Name Search
Salislon may be available in the countries listed below.
Cefadroxil is reported as an ingredient of Salislon in the following countries:
International Drug Name Search
Accidental overdose of products that contain iron is a leading cause of fatal poisoning in children younger than 6 years old. Keep this and all medicines out of the reach of children and away from pets. In case of accidental ingestion, call a doctor or poison control center right away.
Treating or preventing low levels of vitamins and iron in the body.
Multivitamin with Iron Suspension is a vitamin and iron supplement. It works by providing extra vitamins and iron to the body when you do not get enough from your diet.
Contact your doctor or health care provider right away if any of these apply to you.
Some medical conditions may interact with Multivitamin with Iron Suspension. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:
Some MEDICINES MAY INTERACT with Multivitamin with Iron Suspension. Tell your health care provider if you are taking any other medicines, especially any of the following:
This may not be a complete list of all interactions that may occur. Ask your health care provider if Multivitamin with Iron Suspension 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.
Use Multivitamin with Iron Suspension as directed by your doctor. Check the label on the medicine for exact dosing instructions.
Ask your health care provider any questions you may have about how to use Multivitamin with Iron Suspension.
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; dark or discolored stools; diarrhea; nausea; stomach upset.
Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); black, tarry, or bloody stools; severe or persistent nausea, vomiting, or diarrhea; stomach pain or cramping.
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.
Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include black, tarry, or bloody stools; bloody vomit; fast heartbeat; paleness of the skin; seizures; severe diarrhea, nausea, vomiting, or stomach pain; shallow, rapid breathing; sluggishness; unusual drowsiness; weakness.
Store Multivitamin with Iron Suspension at room temperature, between 59 and 86 degrees F (15 and 30 degrees C), in the original container. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Multivitamin with Iron Suspension out of the reach of children and away from pets.
This information is a summary only. It does not contain all information about Multivitamin with Iron Suspension. 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.
Generic Name: melphalan (MEL fa lan)
Brand Names: Alkeran, Alkeran I.V.
Melphalan is a cancer medication. Melphalan interferes with the growth of cancer cells and slows their growth and spread in the body.
Melphalan is used to treat multiple myeloma (a type of blood cancer), cancer of the ovary, and breast cancer.
Melphalan may also be used for other purposes not listed in this medication guide.
Melphalan can cause serious side effects, including: decreased bone marrow function and blood problems (easy bruising or bleeding, unusual weakness, fever, chills, body aches, flu symptoms, bloody or black stools, pale or yellowed skin, confusion or weakness); breathing problems; or liver damage (nausea, stomach pain, low fever, loss of appetite, dark urine, clay-colored stools, jaundice [yellowing of the skin or eyes]). Call your doctor at once if you have any of these side effects.
In some cases, second cancers have been reported to occur during and after treatment with melphalan. Talk to your doctor about your individual risk and benefit of this medication.
Before using melphalan, tell your doctor if you have:
decreased bone marrow (from other diseases or medications).
If you have any of these conditions, you may not be able to use melphalan, or you may need a dosage adjustment or special tests during treatment.
This medication can affect fertility (your ability to have children), whether you are a man or a woman.
Take this medication exactly as it was prescribed for you. Do not take the medication in larger or smaller amounts, or take it for longer than recommended by your doctor. Follow the directions on your prescription label.
Your doctor may occasionally change your dose to make sure you get the best results from this medication.
Melphalan injection is given through a needle placed into a vein. Your doctor, nurse, or other healthcare provider will give you this injection in a clinic or hospital setting.
Melphalan is usually given for a few weeks at a time, followed by a 4-week period off the drug, during which your blood is tested to see how your body responded to the medication. Your doctor will determine how often you use melphalan and for how long. Follow your doctor's instructions carefully.
Melphalan can lower the blood cells that help your body fight infections. This can make it easier for you to bleed from an injury or get sick from being around others who are ill. To be sure your blood cells do not get too low, your blood will need to be tested on a regular basis. It is important that you not miss any scheduled visits to your doctor.
Call your doctor for instructions if you miss a dose of melphalan.
Overdose symptoms may include severe nausea, vomiting, diarrhea, mouth sores, bloody or black stools, coughing up blood or vomit that looks like coffee grounds.
Avoid contact with people who have colds, the flu, or other contagious illnesses. Contact your doctor immediately if you develop signs of infection.
Do not receive a "live" vaccine while you are being treated with melphalan, and avoid coming into contact with anyone who has recently received a live vaccine. There is a chance that the virus could be passed on to you.
easy bruising or bleeding, unusual weakness;
fever, chills, body aches, flu symptoms;
nausea, stomach pain, low fever, loss of appetite, dark urine, clay-colored stools, jaundice (yellowing of the skin or eyes);
missed menstrual periods;
unusual lumps or masses;
red skin rash, rapid pulse, pain, weight loss;
breathing problems or a cough that won't go away; or
pale or yellowed skin, dark colored urine, confusion and weakness.
Less serious side effects may include:
mild nausea, vomiting, diarrhea;
white patches or sores inside your mouth or on your lips;
temporary hair loss; or
mild skin itching and rash.
In some cases, second cancers have been reported to occur during and after treatment with melphalan. Talk to your doctor about your individual risk and benefit in using this medication.
This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.
Before taking melphalan, tell your doctor if you are being treated with any other medicines that weaken your immune system, such as:
cyclosporine (Gengraf, Neoral, Sandimmune);
radiation therapy;
steroids (prednisone and others); or
another chemotherapy medicine.
This list is not complete and there may be other drugs that can interact with melphalan. Tell your doctor about all the prescription and over-the-counter medications you use. This includes vitamins, minerals, herbal products, and drugs prescribed by other doctors. Do not start using a new medication without telling your doctor.
See also: Alkeran I.V. side effects (in more detail)
