Methotrexate Paranova may be available in the countries listed below.
Methotrexate is reported as an ingredient of Methotrexate Paranova in the following countries:
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Haldol Decanoato may be available in the countries listed below.
Haloperidol decanoate (a derivative of Haloperidol) is reported as an ingredient of Haldol Decanoato in the following countries:
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Petscription Triplegard may be available in the countries listed below.
In some countries, this medicine may only be approved for veterinary use.
Permethrin is reported as an ingredient of Petscription Triplegard in the following countries:
Piperonyl Butoxide is reported as an ingredient of Petscription Triplegard in the following countries:
Pyrethrin I is reported as an ingredient of Petscription Triplegard in the following countries:
Pyriproxyfen is reported as an ingredient of Petscription Triplegard in the following countries:
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Promel may be available in the countries listed below.
Metamizole sodium monohydrate (a derivative of Metamizole) is reported as an ingredient of Promel in the following countries:
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Hi-Tac may be available in the countries listed below.
Ranitidine hydrochloride (a derivative of Ranitidine) is reported as an ingredient of Hi-Tac in the following countries:
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Sannax may be available in the countries listed below.
Diclofenac sodium salt (a derivative of Diclofenac) is reported as an ingredient of Sannax in the following countries:
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Sedo-Febril Pediatrico may be available in the countries listed below.
Paracetamol is reported as an ingredient of Sedo-Febril Pediatrico in the following countries:
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Generic Name: dimethyl sulfoxide (dye METH il sul FOX ide)
Brand Names: Rimso-50
Dimethyl sulfoxide is used to treat pain and swelling associated with bladder or urinary conditions including cystitis (bladder inflammation or irritation).
Dimethyl sulfoxide may also be used for other purposes not listed in this medication guide.
Before you receive dimethyl sulfoxide, tell your doctor if you have cancer of your bladder or kidneys. You may not be able to use this medication, or you may need a dose adjustment or special tests during treatment.
You may notice a garlic- or onion-like taste in your mouth while you are receiving dimethyl sulfoxide. This effect may last for several hours after you receive the medication, and you may also sense these odors on your breath or skin. This is a normal side effect of dimethyl sulfoxide and is not cause for alarm.
Before you receive dimethyl sulfoxide, tell your doctor if you have cancer of your bladder or kidneys. You may not be able to use this medication, or you may need a dose adjustment or special tests during treatment.
Dimethyl sulfoxide is injected directly into the bladder using a catheter or syringe inserted into the urethra (the tube for passing urine out of your bladder). You will receive this medication in a clinic or hospital setting.
After dimethyl sulfoxide is placed into the bladder, you will need to hold the medication in for 15 minutes before emptying your bladder.
Dimethyl sulfate is usually given once every 2 weeks until your symptoms are relieved. Follow your doctor's instructions about your specific dosing schedule.
Your doctor may also recommend other medications to treat pain or bladder spasm. Be sure to read the medication guide or patient instructions provided with each of your medications.
To be sure this medication is helping your condition and not causing harmful effects, your blood will need to be tested on a regular basis. You may also need to have eye exams before and during treatment. Do not miss any scheduled appointments.
Call your doctor for instructions if you miss an appointment for your dimethyl sulfoxide treatment.
An overdose of dimethyl sulfoxide is not expected to produce life-threatening symptoms.
Follow your doctor's instructions about any restrictions on food, beverages, or activity while you are being treated with dimethyl sulfoxide.
Tell your caregivers if you feel severe discomfort or irritation when the medication is inserted or while you are holding it in your bladder. This discomfort may become less noticeable over time with repeat treatments.
You may notice a garlic- or onion-like taste in your mouth while you are receiving dimethyl sulfoxide. This effect may last for several hours after you receive the medication, and you may also sense these odors on your breath or skin. This is a normal side effect of dimethyl sulfoxide and is not cause for concern.
This is not a complete list of side effects and others may occur. Tell your doctor about any unusual or bothersome side effect. You may report side effects to FDA at 1-800-FDA-1088.
There may be other drugs that can interact with dimethyl sulfoxide. 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.
See also: Rimso-50 side effects (in more detail)
Isosorbide Mononitrato Dorom may be available in the countries listed below.
Isosorbide Mononitrate is reported as an ingredient of Isosorbide Mononitrato Dorom in the following countries:
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bue-PROE-pee-on
Wellbutrin(R) formulations and Forfivo XL: Antidepressants increased the risk of suicidal thinking and behavior in children, adolescents, and young adults in short-term studies with major depressive disorder (MDD) and other psychiatric disorders. Short-term studies did not show an increase in the risk of suicidality with antidepressants compared to placebo in adults beyond age 24, and there was a reduction in risk with antidepressants compared to placebo in adults aged 65 and older. This risk must be balanced with the clinical need. Monitor patients closely for clinical worsening, suicidality, or unusual changes in behavior. Families and caregivers should be advised of the need for close observation and communication with the prescriber. Not approved for use in pediatric patients. Zyban(R): Serious neuropsychiatric events, including depression, suicidal ideation, suicide attempt, and completed suicide, have been reported in patients with and without preexisting psychiatric disease who were taking bupropion for smoking cessation; some experienced worsening of their psychiatric illnesses. All patients should be observed for changes in behavior, hostility, agitation, depressed mood, and suicide-related events, including ideation, behavior, and attempted suicide. The patient should stop taking bupropion and contact a healthcare provider immediately if any neuropsychiatric behavior that is not typical for the patient is observed, or if the patient develops suicidal ideation or suicidal behavior. This risk should be weighed against the benefits of its use .
Antidepressants increased the risk of suicidal thinking and behavior in children, adolescents, and young adults in short-term studies with major depressive disorder (MDD) and other psychiatric disorders. Short-term studies did not show an increase in the risk of suicidality with antidepressants compared to placebo in adults beyond age 24, and there was a reduction in risk with antidepressants compared to placebo in adults aged 65 and older. This risk must be balanced with the clinical need. Monitor patients closely for clinical worsening, suicidality, or unusual changes in behavior. Families and caregivers should be advised of the need for close observation and communication with the prescriber. Not approved for use in pediatric patients .
In the U.S.
Available Dosage Forms:
Therapeutic Class: Antidepressant
Chemical Class: Aminoketone
Bupropion is used to treat mental depression. It is also used as part of a support program to help people stop smoking. bupropion may also be used to prevent depression in patients with seasonal affective disorder, which is sometimes called winter depression.
Bupropion is sold under different brand names for different uses. If you are already taking medicine for mental depression or to help you stop smoking, discuss this with your doctor before taking bupropion. It is very important that you receive only one prescription for bupropion at a time.
bupropion 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 bupropion, the following should be considered:
Tell your doctor if you have ever had any unusual or allergic reaction to bupropion 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 bupropion in the pediatric population. Studies with other medicines used for depression have shown that some children, teenagers, and young adults think about suicide or attempt suicide when taking these medicines. Because of this toxicity, use in children is not recommended.
Appropriate studies performed to date have not demonstrated geriatric-specific problems that would limit the usefulness of bupropion in the elderly. However, elderly patients may be more sensitive to the effects of bupropion than younger adults, and are more likely to have age-related kidney or liver problems, which may require caution and an adjustment in the dose for patients receiving bupropion.
| 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 bupropion, 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 bupropion 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 bupropion 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.
Using bupropion 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. The following interactions have been selected on the basis of their potential significance and are not necessarily all-inclusive.
Using bupropion with any of the following is usually not recommended, but may be unavoidable in some cases. If used together, your doctor may change the dose or how often you use bupropion, or give you special instructions about the use of food, alcohol, or tobacco.
The presence of other medical problems may affect the use of bupropion. Make sure you tell your doctor if you have any other medical problems, especially:
Use bupropion only as directed by your doctor. Do not use more of it, do not use it more often, and do not use it for a longer time than your doctor ordered. To do so, may increase the chance of side effects.
bupropion should come with a Medication Guide. Read and follow these instructions carefully. Ask your doctor if you have any questions.
Use only the brand of bupropion that your doctor prescribed. Different brands may not work the same way.
Swallow the sustained-release tablets whole. Do not break, crush, divide, or chew it.
You may take bupropion with or without food. But, if you have nausea, take bupropion with food.
To lessen stomach upset, bupropion may be taken with food, unless your doctor has told you to take it on an empty stomach.
If you are taking Zyban® tablets to help you stop smoking, you may continue to smoke for about 1 week after you start using bupropion. Then, you should set a target date to quit smoking during your second week of Zyban® treatment. Talk to your doctor if you are having trouble to stop smoking after you have used bupropion for at least 7 weeks.
Do not smoke if you are using a nicotine patch or any other medicine containing nicotine together with Zyban® tablets. To do so, may increase risk for more serious side effects.
bupropion must be taken for several weeks, usually 4 weeks, before you start to feel better. You will probably need to keep taking bupropion for several months to help prevent the return of your depression. Your doctor will check your progress at regular visits, especially during the first few weeks that you take bupropion.
If you have trouble with sleeping (insomnia), do not take bupropion too close to bedtime.
For patients taking the extended-release tablet form of bupropion:
To help you remember to use your medicine, take it at the same time each day.
The dose of bupropion 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 bupropion. 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 bupropion, skip the missed dose and go back to your regular dosing schedule. Do not double doses.
If you are taking the extended-release tablets and you miss a dose, skip the missed dose and go back to your regular dosing schedule.
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.
Your doctor will check your progress at regular visits, especially during the first few months that you take bupropion. The amount of bupropion you take may have to be adjusted to meet the needs of your condition and to help avoid unwanted effects.
Do not take bupropion with or within 14 days of taking a drug with monoamine oxidase inhibitor (MAOI) activity (e.g., isocarboxazid [Marplan®], phenelzine [Nardil®], procarbazine [Matulane®], selegiline [Eldepryl®], or tranylcypromine [Parnate®]). Do not take an MAO inhibitor within 14 days of taking bupropion. If you do, you might have convulsions (seizures).
Your blood pressure might get too high while you are using bupropion. This may cause headaches, blurred vision, and other symptoms. You might need to measure your blood pressure at home. If you think your blood pressure is getting too high, call your doctor right away.
Bupropion may cause some people to be agitated, irritable, or display other abnormal behaviors. It may also cause some people to have suicidal thoughts and tendencies or to become more depressed. Make sure the doctor knows if you have trouble sleeping, get upset easily, have a big increase in energy, or start to act reckless. Also tell the doctor if you have sudden or strong feelings, such as feeling nervous, angry, restless, violent, or scared. If you or your caregiver notice any of these side effects, tell your doctor right away.
bupropion may cause a serious type of allergic reaction called anaphylaxis. Anaphylaxis can be life-threatening and requires immediate medical attention. Stop using bupropion and tell your doctor right away if you have a rash; itching; swelling of the face, tongue, and throat; trouble breathing; or chest pain after you take bupropion.
Serious skin reactions can occur with bupropion. Check with your doctor right away if you have blistering, peeling, or loosening of the skin; red skin lesions; severe acne or skin rash; sores or ulcers on the skin; or fever or chills while you are using bupropion.
Drinking alcoholic beverages should be limited or avoided, if possible, while taking bupropion. This will help prevent seizures.
bupropion may cause some people to have a false sense of well-being, or to become drowsy, dizzy, or less alert than they are normally. Make sure you know how you react to bupropion before you drive, use machines, or do anything else that could be dangerous if you are dizzy or not alert and clearheaded.
Do not stop taking bupropion without checking first with your doctor. Your doctor may want you to gradually reduce the amount you are taking before stopping it completely. This is to decrease the chance of having side effects such as agitation, anxiety, dizziness, a feeling of constant movement of self or surroundings, headache, increased sweating, nausea, trembling or shaking, trouble with sleeping or walking, or unusual tiredness when you stop the medicine.
Check with your doctor right away if you have pain or tenderness in the upper stomach; pale stools; dark urine; loss of appetite; nausea; unusual tiredness or weakness; or yellow eyes or skin. These could be symptoms of a serious liver problem.
bupropion may cause changes in your appetite or weight. Your doctor may need to check your weight regularly during treatment with bupropion.
Before you have any medical tests, tell the medical doctor in charge that you are taking bupropion. The results of some tests may be affected by bupropion.
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:
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: bupropion side effects (in more detail)
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Hypoloc may be available in the countries listed below.
Nebivolol hydrochloride (a derivative of Nebivolol) is reported as an ingredient of Hypoloc in the following countries:
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Amotein may be available in the countries listed below.
Metronidazole is reported as an ingredient of Amotein in the following countries:
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Relieving symptoms of sinus congestion, pressure, runny nose, and sneezing due to colds, upper respiratory infections, and allergies. It may also be used for other conditions as determined by your doctor.
Rhinacon A Controlled-Release Tablets are an antihistamine and decongestant combination. The antihistamine works by blocking the action of histamine, which helps reduce symptoms such as watery eyes and sneezing. The decongestant promotes sinus and nasal drainage, which relieves congestion and pressure.
Contact your doctor or health care provider right away if any of these apply to you.
Some medical conditions may interact with Rhinacon A Controlled-Release Tablets. 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 Rhinacon A Controlled-Release Tablets. 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 Rhinacon A Controlled-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.
Use Rhinacon A Controlled-Release Tablets 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 Rhinacon A Controlled-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; excitability; headache; loss of appetite; nausea; nervousness or anxiety; trouble sleeping; upset stomach; vomiting; weakness.
Severe allergic reactions (rash; hives; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); difficulty urinating or inability to urinate; fast or irregular heartbeat; hallucinations; seizures; severe dizziness, lightheadedness, or headache; tremor; trouble sleeping; vision changes.
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: Rhinacon A side effects (in more detail)
Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center (http://www.aapcc.org ), 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 Rhinacon A Controlled-Release Tablets 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 Rhinacon A Controlled-Release Tablets out of the reach of children and away from pets.
This information is a summary only. It does not contain all information about Rhinacon A Controlled-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.
Azithin may be available in the countries listed below.
Azithromycin is reported as an ingredient of Azithin in the following countries:
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