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Generic Tofranil(Generic name: Imipramine Hydrochloride)
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Tofranil Overview |
Tofranil (generic name Imipramine Hydrochloride) is anti-depressant medicine.
Information about Tofranil such as Tofranil usage, Tofranil side effects, detailed Tofranil description and other you may find on our online pharmacy. You may order Tofranil on our site. We guarantee: lowest Tofranil price, free shipping, free calls for customers, highest level of security, live support. Our online medical support will give you a free consultation to receive the prescription on the concrete medicine in accordance with your disease.
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| Tofranil Description |
brand name: Tofranil
generic names: Imipramine, Imipramine hydrochloride
Why is Tofranil prescribed? Tofranil is used to treat depression. It is a member of the family of drugs called tricyclic antidepressants. Tofranil is also used on a short-term basis, along with behavioral therapies, to treat bed-wetting in children aged 6 and older. Its effectiveness may decrease with longer use. Some doctors also prescribe Tofranil to treat bulimia, attention deficit disorder in children, obsessive-compulsive disorder, and panic disorder. Tofranil-PM, which is usually taken once daily at bedtime, is approved to treat major depression.
What are Imipramine (Tofranil) tablets? Imipramine (Tofranil ® ) is an antidepressant. Imipramine can help to lift your spirits by treating your depression. Imipramine (Tofranil) can help children who have a nighttime bed-wetting problem. Generic Imipramine tablets are available.
Imipramine (Tofranil) side effects Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat. Call your doctor at once if you have any new or worsening symptoms such as: mood or behavior changes, irritable, agitated, hostile, aggressive, restless, hyperactive (mentally or physically), more depressed, or if you feel impulsive, trouble sleeping, panic attacks, anxiety. Call your doctor at once if you have any of these serious side effects: - skin rash, pain, numbness, severe tingling, bruising, or muscle weakness.
- extreme thirst with headache, vomiting, nausea, and weakness;
- urinating more or less than usual;
- restless muscle movements in your eyes, jaw, tongue, or neck;
- easy bruising or bleeding, unusual weakness;
- confusion, hallucinations, or seizure (convulsions);
- swelling, rapid weight gain;
- feeling short of breath, even with mild exertion;
- sudden headache, speech, problems with vision, confusion, or balance;
- sudden numbness or weakness, especially on one side of the body;
- chest pain or heavy feeling, pain spreading to the arm or shoulder, nausea, sweating, general ill feeling;
- fast, pounding, or uneven heart rate;
Less serious side effects may be more likely to occur, such as: - decreased sex drive, impotence, or difficulty having an orgasm.
- breast swelling (in men or women); or
- blurred vision, headache, ringing in your ears;
- nightmares;
- feeling dizzy, drowsy, or tired;
- weakness, lack of coordination;
- weight changes;
- dry mouth, unpleasant taste;
- constipation or diarrhea;
- nausea, vomiting, stomach pain, loss of appetite;
Side effects other than those listed here may also occur. Talk to your doctor about any side effect that seems unusual or that is especially bothersome.
How can this medicine affect other medicines? It is important to tell your doctor or pharmacist what medicines you are already taking, including those bought without a prescription and herbal medicines, before you start treatment with this medicine. Similarly, check with your doctor or pharmacist before taking any new medicines while taking this one, to ensure that the combination is safe . Imipramine should not be taken in combination with a monoamine oxidase inhibitor antidepressant (MAOI), isocarboxazid, tranylcypromine, eg phenelzine, or moclobemide. Treatment with Imipramine (Tofranil) should not be started until at least three weeks after stopping an MAOI. Conversely, an MAOI should not be started until three weeks after stopping Imipramine. Moclobemide should not be started until at least a week after stopping Imipramine (Tofranil). If Imipramine is taken with other medicines that enhance serotonin activity in the brain, there may be an increased risk of side effects such as increased heart rate and diarrhoea, shivering, tremor, agitation, known collectively as the 'serotonin syndrome'. Other medicines that increase serotonin activity include the following: There may be an increased risk of side effects such as difficulty passing urine and blurred vision if Imipramine (Tofranil) is taken with other medicines that have anticholinergic effects, dry mouth, constipation, - antisickness medicines, eg meclozine, cyclizine.
- muscle relaxants, eg baclofen
- certain other antidepressants
- antiarrhythmics, eg disopyramide, propafenone
- antipsychotics, eg chlorpromazine, clozapine (some antipsychotics may also increase the blood level of Imipramine (Tofranil))
- antispasmodics, eg hyoscine, atropine
- antihistamines, eg promethazine, chlorphenamine
- anticholinergics for Parkinson's disease, eg procyclidine, trihexyphenidyl
- anticholinergics for urinary incontinence, eg tolterodine, oxybutynin
There may be an increased risk of side effects on the heart if Imipramine (Tofranil) is taken in combination with the following medicines; these medicines should be avoided in people taking Imipramine: - pentamidine.
- moxifloxacin
- the antimalarials halofantrine, chloroquine or quinine
- the antihistamines astemizole, terfenadine or mizolastine
- certain antipsychotics, eg thioridazine, haloperidol, pimozide
- medicines to treat abnormal heart rhythms, eg amiodarone, procainamide, quinidine, disopyramide, sotalol
- atomoxetine
There may be an increased risk of drowsiness if Imipramine (Tofranil) is taken in combination with other medicines that can cause drowsiness, such as the following: - strong opioid painkillers, such as morphine, codeine.
- sleeping tablets, eg zopiclone
- benzodiazepines, eg diazepam, temazepam
- sedating antihistamines, eg chlorphenamine
Imipramine (Tofranil) reduces the blood pressure lowering effect of clonidine and guanethidine. There may be a sudden and marked increase in blood pressure and heart rate if adrenaline, noradrenaline or phenylephrine are given by injection to people taking Imipramine. These medicines should be avoided in people taking Imipramine (Tofranil). Imipramine may alter the anti-blood-clotting effect of anticoagulant medicines such as warfarin. Your blood clotting time (INR) should be carefully monitored if you are taking these two medicines together. The following medicines may increase the blood level of Imipramine, which could increase the risk of side effects: - terbinafine.
- SSRI antidepressants such as fluvoxamine and fluoxetine
- ritonavir
- quinidine
- propranolol
- oestrogen-containing contraceptives (these may also decrease the antidepressant effect of Imipramine (Tofranil))
- methylphenidate
- labetolol
- disulfiram
- cimetidine
- calcium channel blockers such as diltiazem or verapamil
The following medicines may decrease the blood level of Imipramine (Tofranil) and make it less effective: - rifampicin.
- barbiturates such as phenobarbital
If you experience a dry mouth as a side effect of this medicine you may find that medicines that are designed to dissolve and be absorbed from under the tongue, eg sublingual glyceryl trinitrate (GTN) tablets for angina, become less effective. This is because the tablets do not dissolve properly in a dry mouth. To resolve this, drink a mouthful of water before taking sublingual tablets.
Special information if you are pregnant or breastfeeding The effects of Tofranil during pregnancy have not been adequately studied. Pregnant women should use Tofranil only when the potential benefits clearly outweigh the potential risks. If you are pregnant or plan to become pregnant, inform your doctor immediately. Tofranil may appear in breast milk and could affect a nursing infant. If this medication is essential to your health, your doctor may advise you to stop breastfeeding until your treatment is finished.
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