Spasmoson may be available in the countries listed below.
Ingredient matches for Spasmoson
Scopolamine is reported as an ingredient of Spasmoson in the following countries:
- Bangladesh
International Drug Name Search
Spasmoson may be available in the countries listed below.
Scopolamine is reported as an ingredient of Spasmoson in the following countries:
International Drug Name Search
Flunazul may be available in the countries listed below.
Fluconazole is reported as an ingredient of Flunazul in the following countries:
International Drug Name Search
Definition of Costochondritis: Costochondritis is an inflammation of a rib or the cartilage connecting a rib and is a common cause of chest pain.
The following drugs and medications are in some way related to, or used in the treatment of Costochondritis. This service should be used as a supplement to, and NOT a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners.
Medical Encyclopedia:
Generic Name: bacitracin ophthalmic (BAS i TRAY sin off THAL mik)
Brand names: Ocu-Tracin, AK-Tracin
Bacitracin is an antibiotic that kills bacteria.
Bacitracin ophthalmic may also be used for other purposes not listed in this medication guide.
Before using bacitracin ophthalmic, tell your doctor if you have any type of viral or fungal infection in your eye. Bacitracin is for treating only bacterial infections.
Do not use any other eye medications unless your doctor has prescribed them.
Bacitracin ophthalmic can cause temporary blurred vision. Be careful if you drive or do anything that requires you to be able to see clearly.
Use this medication for the full prescribed length of time. Your symptoms may improve before the infection is completely cleared. Bacitracin will not treat a viral or fungal infection of the eye.
Before using bacitracin ophthalmic, tell your doctor if you have any type of viral or fungal infection in your eye. Bacitracin is for treating only bacterial infections.
Use this medication exactly as prescribed by your doctor. Do not use it in larger amounts or for longer than recommended. Follow the directions on your prescription label.
Wash your hands before using bacitracin ophthalmic ointment.
You may warm the ointment by holding the medicine tube in your hand for a few minutes before use. Tilt your head back slightly and pull down gently on your lower eyelid. Apply a thin film of the ointment into your lower eyelid. Close your eye and roll your eyeball around for 1 to 2 minutes.
Use this medication for the full prescribed length of time. Your symptoms may improve before the infection is completely cleared. Bacitracin will not treat a viral or fungal infection of the eye.
Use the medication as soon as you remember the missed dose. If it is almost time for your next dose, skip the missed dose and use the medicine at your next regularly scheduled time. Do not use extra medicine to make up the missed dose.
An overdose of bacitracin ophthalmic is not likely to occur.
Do not use any other eye medications unless your doctor has prescribed them.
Bacitracin ophthalmic can cause temporary blurred vision. Be careful if you drive or do anything that requires you to be able to see clearly.
Less serious side effects may include temporary blurred vision.
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 bacitracin ophthalmic used in the eyes. But many drugs can interact with each other. Tell your doctor about all your prescription and over-the-counter medications, vitamins, minerals, herbal products, and drugs prescribed by other doctors. Do not start a new medication without telling your doctor.
Betametasona Fosfato Disodico may be available in the countries listed below.
Betamethasone 21-(disodium phosphate) (a derivative of Betamethasone) is reported as an ingredient of Betametasona Fosfato Disodico in the following countries:
International Drug Name Search
Adelone may be available in the countries listed below.
Prednisolone 21-acetate (a derivative of Prednisolone) is reported as an ingredient of Adelone in the following countries:
International Drug Name Search
Acetylsalicylzuur may be available in the countries listed below.
In some countries, this medicine may only be approved for veterinary use.
Acetylsalicylic Acid is reported as an ingredient of Acetylsalicylzuur in the following countries:
International Drug Name Search
Lisinopril / Hydrochlorothiazide CF may be available in the countries listed below.
Hydrochlorothiazide is reported as an ingredient of Lisinopril / Hydrochlorothiazide CF in the following countries:
Lisinopril dihydrate (a derivative of Lisinopril) is reported as an ingredient of Lisinopril / Hydrochlorothiazide CF in the following countries:
International Drug Name Search
Amisulprid Teva may be available in the countries listed below.
Amisulpride is reported as an ingredient of Amisulprid Teva in the following countries:
International Drug Name Search
Amantadin Holsten may be available in the countries listed below.
Amantadine hydrochloride (a derivative of Amantadine) is reported as an ingredient of Amantadin Holsten in the following countries:
International Drug Name Search
Vi-Gel may be available in the countries listed below.
Indometacin is reported as an ingredient of Vi-Gel in the following countries:
International Drug Name Search
Omeprazolo Alter may be available in the countries listed below.
Omeprazole is reported as an ingredient of Omeprazolo Alter in the following countries:
International Drug Name Search
Cardipine may be available in the countries listed below.
Isosorbide Dinitrate is reported as an ingredient of Cardipine in the following countries:
International Drug Name Search
Notorium may be available in the countries listed below.
Bromazepam is reported as an ingredient of Notorium in the following countries:
International Drug Name Search
Generic Name: naltrexone (Oral route)
nal-TREX-one
Can cause hepatocellular injury when given in excessive doses. Contraindicated in acute hepatitis or liver failure, and its use in patients with active liver disease must be carefully considered in light of its hepatotoxic effects. Patients should be warned of the risk of hepatic injury and advised to stop the use of naltrexone and seek medical attention if they experience symptoms of acute hepatitis .
In the U.S.
Available Dosage Forms:
Therapeutic Class: Toxicology-Antidote Agent
Pharmacologic Class: Opioid Antagonist
Naltrexone is used to help narcotic addicts who have stopped taking narcotics to stay drug-free. It is also used to help alcoholics stay alcohol-free. The medicine is not a cure for addiction. It is used as part of an overall program that may include counseling, attending support group meetings, and other treatment recommended by your doctor.
Naltrexone is not a narcotic. It works by blocking the effects of narcotics, especially the "high'' feeling that makes you want to use them. It also may block the "high'' feeling that may make you want to use alcohol. It will not produce any narcotic-like effects or cause mental or physical dependence. It will not prevent you from becoming impaired while drinking alcohol.
Naltrexone will cause withdrawal symptoms in people who are physically dependent on narcotics. Therefore, naltrexone treatment is started after you are no longer dependent on narcotics. The length of time this takes may depend on which narcotic you took, the amount you took, and how long you took it. Before you start taking this medicine, be sure to tell your doctor if you think you are still having withdrawal symptoms.
Naltrexone 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 naltrexone in the pediatric population. Safety and efficacy have not been established.
Appropriate studies performed to date have not demonstrated geriatric-specific problems that would limit the usefulness of naltrexone in the elderly.
| 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. 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 is not recommended. Your doctor may decide not to treat you with this medication or change some of the other medicines you take.
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.
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:
Take naltrexone regularly as ordered by your doctor. It may be helpful to have someone else, such as a family member, doctor, or nurse, give you each dose as scheduled.
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.
Call your doctor or pharmacist for instructions.
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. Your doctor may want to do certain blood tests to see if the medicine is causing unwanted effects.
Remember that use of naltrexone is only part of your treatment. Be sure that you follow all of your doctor's orders, including seeing your therapist and/or attending support group meetings on a regular basis.
Do not try to overcome the effects of naltrexone by taking narcotics. To do so may cause coma or death. You may be more sensitive to the effects of narcotics than you were before beginning naltrexone therapy.
Naltrexone also blocks the useful effects of narcotics. Always use a non-narcotic medicine to treat pain, diarrhea, or a cough. If you have any questions about the proper medicine to use, check with your doctor.
Naltrexone will not prevent you from becoming impaired when you drink alcohol. Do not take naltrexone in order to drive or perform other activities while under the influence of alcohol.
Never share this medicine with anyone else, especially someone who is using narcotics. Naltrexone causes withdrawal symptoms in people who are using narcotics.
Tell all medical doctors, dentists, and pharmacists you go to that you are taking naltrexone.
It is recommended that you carry identification stating that you are taking naltrexone. Identification cards may be available from your doctor.
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:
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:
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: Revia side effects (in more detail)
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