What are the side effects for imipramine
A:A few adverse reactions which have not been reported with this specific drug, but may be:Cardiovascular: Orthostatic hypotension, hypertension, tachycardia, palpitation, myocardial infarction, arrhythmias, heart block, ECG changes….MORE? [ Source: http://www.chacha.com/question/what-are-the-side-effects-for-imipramine ]
More Answers to “What are the side effects for imipramine“
- What Are The Side Effects Of Imipramine
- Lifestyle treatment of narcolepsy includes taking three or more scheduled sleep-times throughout the day. One study suggested that the best approach is a combination of scheduled nighttime sleep and two 15-minute naps (for example one befor…
- How about side effects of Tofranil ?
- 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…
- What are the possible side effects of Imipramine?
- Call your doctor at once if you have any new or worsening symptoms such as: mood or behavior changes, anxiety, panic attacks, trouble sleeping, or if you feel impulsive, irritable, agitated, hostile, aggressive, restless, hyperactive (menta…
Related Questions Answered on Y!Answers
- what are the side effects of slowly reducing and then stopping intake of imipramine?
- Q: My doctor noticed heart skips, and talked to my psychiatrist. They agreed to reduce, and within the month, have me stop taking Imipramine. I was taking 300 mg a night. Last night I started taking 200 mg, and will for the next 7 days. Then down to 100 mg for 7 days. And finally down to 50 mg for 2 weeks. I’d like to know, based on this reducing regimen, what side effects I could expect. And as a side note…maybe you can suggest an antidepressant that works well for you. Thanks, Bill.
- A: Imipramine/Tofrinil can cause heart beat irregularities. Try one of the new SSRIs. I like Lexapro but I think there are even newer ones available out there. It sounds like you are doing it right though, being monitored by a psychiatrist. You should never stop taking prescription medication on your own.
- What is the the best anti depressant that has the least side effects and safest long term?
- Q: I have trouble sleeping and suffer occasional panic attacks and daily anxiety. My doctor gave me imipramine (Tofranil) and its just been 2 days and i am experiencing shallow breathing. I also read about heart issues, if im going to be on something for life i dont want a drug that can create a heart problem! Any long term experience with anti depressants, anyone?I run 2 miles everyday and lift weight 5 times a week 🙂
- A: I’ve been on about 8 different types and they all cause side effects. There have been stories in the media where perfectly normal people (apart from having depression) have gone insane on them and killed someone (an elderly man murdered his wife after taking Zoloft and he had no history of violent behaviour or trouble with the law).They can also cause suicidal ideation and some people end up commiting suicide after taking certain types. This is why it is very important to inform your doctor of any negative side effects that may be concerning you.The one that worked best for me (because it is also great for anxiety and cured my panic attacks) is Cymbalta. However, you need to be very careful with drinking alcohol on this medication as it increases the risk of serious liver damage. Having said that, you should only drink in strict moderation on any antidepressant.If you only drink in moderation (being 2-4 drinks a couple of times a week max) on Cymbalta it is very safe although as with any antidepressant, there is always a small percentage of patients who will experience serious side effects.For me antidepressants have stopped me attempting suicide every couple of months and self harming as well as allowed me to work and socialise again so the benefits far outweigh any side effects.
- Could anyone tell me the effect of Imipramine ?
- Q: I know of a person who is taking Imipramine tablets for some illness called “Mild Depression” . Could any one tell me the effects and side effects. What will happen in taking an over dosage.
- A: AntidepressantImipramine is a tricyclic antidepressant with general pharmacological properties similar to those of structurally related tricyclic antidepressant drugs such as amitriptyline and doxepin. It possesses anticholinergic properties which are responsible for certain of its side effects. The mechanism of action of imipramine and other tricyclic antidepressants is not well established, but it is thought that it might be related to their action on the transmitter-uptake mechanism of monoaminergic neurons. The mechanism of action in childhood nocturnal enuresis is not fully known. Imipramine is well absorbed from the gastrointestinal tract. Following oral administration of 50 mg 3 times daily for 10 days, the mean steady-state plasma concentration was 33 to 85 ng/mL for imipramine and 43 to 109 ng/mL for desmethylimipramine, an active metabolite. Peak plasma levels are reached in 2 to 5 hours, and plasma half-life ranges from 9 to 20 hours. Approximately 86% of imipramine is bound to plasma proteins. It is excreted primarily as inactive metabolites, up to 80% in the urine and up to 20% in the feces. For the relief of symptoms of depression. Imipramine may also be useful as temporary adjunctive therapy in reducing enuresis in children aged 5 years and older, after possible organic causes have been excluded by appropriate tests. In patients having daytime symptoms of frequency and urgency, examination should include voiding cystourethrography and cytoscopy, as necessary. The effectiveness of treatment may decrease with continued drug administration. For the relief of symptoms of depression. Imipramine may also be useful as temporary adjunctive therapy in reducing enuresis in children aged 5 years and older, after possible organic causes have been excluded by appropriate tests. In patients having daytime symptoms of frequency and urgency, examination should include voiding cystourethrography and cytoscopy, as necessary. The effectiveness of treatment may decrease with continued drug administrationChildren have been reported to be more sensitive than adults to an acute overdosage of imipramine. An acute overdose in infants or young children must be considered serious and potentially fatal. Symptoms:These may vary in severity depending upon factors such as the amount of drug absorbed, the age of the patient and the interval between drug ingestion and the start of treatment. Blood and urine levels of imipramine may not reflect the severity of poisoning; they have chiefly a qualitative rather than quantitative value, and are unreliable indicators in the clinical management of the patient. Drowsiness, stupor, ataxia, vomiting, cyanosis, restlessness, agitation, delirium, severe perspiration, hyperactive reflexes, muscle rigidity, athetoid movements, convulsions, respiratory depression, hyperpyrexia, hypothermia, mydriasis, and bowel and bladder paralysis may occur. Serious cardiovascular disturbances are frequently present, including tachycardia, cardiac arrhythmia (flutter, atriofibrillation, ventricular premature beats, and ventricular tachycardia), as well as impaired myocardial conduction, atrioventricular and intraventricular block, ECG abnormalities (such as widened QRS complexes and marked S-T shifts and signs of congestive heart failure and cardiac arrest). Hypotension and initial hypertension may occur. However, the usual finding is increasing hypotension which may lead eventually to shock. Coma may ensue. Treatment:Symptomatic and supportive. Cardiac arrhythmias and CNS involvement pose the greatest threat with tricyclic antidepressant overdosage and may occur suddenly even when initial symptoms appear to be mild. Therefore, patients who may have ingested an overdosage of imipramine, particularly children, should be hospitalized and kept under close surveillance. If the patient is conscious, induced emesis followed by gastric lavage, with appropriate precautions to prevent pulmonary aspiration, should be accomplished as soon as possible. Following lavage, activated charcoal may be administered to reduce absorption. An adequate airway should be established in comatose patients and assisted ventilation instituted, if necessary, but respiratory stimulants should not be used. Hyperpyrexia should be controlled by external measures, such as ice packs and cooling sponge baths. Acidosis may be treated by cautious administration of sodium bicarbonate. Adequate renal function should be maintained. External stimulation should be minimized to reduce the tendency to convulsions. If convulsions occur, anticonvulsants (preferably i.v. diazepam) should be administered. Barbiturates may intensify respiratory depression, particularly in children, and aggravate hypotension and coma. Paraldehyde may be used in some children to counteract muscular hypertonus and convulsions with less likelihood of causing respiratory depression. If the patient fails to respond r