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Low sperm count...anybody?

Tue, 03/20/2007 - 14:17
Hi. I read on this website that AED,specially carbamazepine and phenytoin, affects sperm count,sperm mobility,fertility etc. Has this affected any of you or anybody you know? What did you do about it? I need advice. Thank you. PS: My husband has E since he was a child and since then he was on phenytoin.He also have taken keppra since last 3years. At the moment he is on keppra and tegretol retard.The phenytoin was been withdrawn.

Comments

Re: Low sperm count...anybody?

Submitted by Bill01 on Mon, 2008-06-30 - 03:39

Hello. I am a bit like Beau below. I have been taking a rather low dose of Tegretol (1 in the mornoing and 2 at night - all 200mgs tablets) and have absolutely no interest in sex at all. I go to bed and am asleep in minutes. I try but there is no interest at all and I am afraid that my wife suffers because of this. And no I haven't mentioned this to either the neurologist or my wife.

That's my experience anyway. Sleep like a log for 9 hours too.

 

Bill.

Hello. I am a bit like Beau below. I have been taking a rather low dose of Tegretol (1 in the mornoing and 2 at night - all 200mgs tablets) and have absolutely no interest in sex at all. I go to bed and am asleep in minutes. I try but there is no interest at all and I am afraid that my wife suffers because of this. And no I haven't mentioned this to either the neurologist or my wife.

That's my experience anyway. Sleep like a log for 9 hours too.

 

Bill.

Re: Low sperm count...anybody?

Submitted by alfreds on Wed, 2009-07-22 - 13:32
Hi, I will recommend an artificial insemination for both of you. Look it doesnt always mattern about the sperm count. Maybe your husband is giving out right number of sperm cells but these cells might not be motile. Visit a specialist and sort out the original problem. Maybe artifical insemination methods might help.

Information on Tegretol

Submitted by GratefulForHelp on Mon, 2008-01-14 - 16:34

Tegretol

Side Effects & Drug Interactions

SIDE EFFECTS

If adverse reactions are of such severity that the drug must be discontinued, the physician must be aware that abrupt discontinuation of any anticonvulsant drug in a responsive epileptic patient may lead to seizures or even status epilepticus with its life-threatening hazards.

The most severe adverse reactions have been observed in the hemopoietic system (see BOXED WARNING), the liver and the cardiovascular system.

The most frequently observed adverse reactions, particularly during the initial phases of therapy, are dizziness, drowsiness, unsteadiness, nausea, and vomiting. To minimize the possibility of such reactions, therapy should be initiated at the low dosage recommended.

The following additional adverse reactions have been reported:

Hemopoietic System: Aplastic anemia, agranulocytosis, pancytopenia, bone marrow depression, thrombocytopenia, leukopenia, leukocytosis, eosinophilia, acute intermittent porphyria.

Skin: Toxic epidermal necrolysis (TEN) and Stevens-Johnson syndrome (SJS) (see BOXED WARNING), pruritic and erythematous rashes, urticaria, photosensitivity reactions, alterations in skin pigmentation, exfoliative dermatitis, erythema multiforme and nodosum, purpura, aggravation of disseminated lupus erythematosus, alopecia, and diaphoresis. In certain cases, discontinuation of therapy may be necessary. Isolated cases of hirsutism have been reported, but a causal relationship is not clear.

Cardiovascular System: Congestive heart failure, edema, aggravation of hypertension, hypotension, syncope and collapse, aggravation of coronary artery disease, arrhythmias and AV block, thrombophlebitis, thromboembolism, and adenopathy or lymphadenopathy.

Some of these cardiovascular complications have resulted in fatalities. Myocardial infarction has been associated with other tricyclic compounds.

Liver: Abnormalities in liver function tests, cholestatic and hepatocellular jaundice, hepatitis; very rare cases of hepatic failure.

Pancreatic: Pancreatitis.

Respiratory System: Pulmonary hypersensitivity characterized by fever, dyspnea, pneumonitis, or pneumonia.

Genitourinary System: Urinary frequency, acute urinary retention, oliguria with elevated blood pressure, azotemia, renal failure, and impotence. Albuminuria, glycosuria, elevated BUN, and microscopic deposits in the urine have also been reported.

Tegretol

Side Effects & Drug Interactions

SIDE EFFECTS

If adverse reactions are of such severity that the drug must be discontinued, the physician must be aware that abrupt discontinuation of any anticonvulsant drug in a responsive epileptic patient may lead to seizures or even status epilepticus with its life-threatening hazards.

The most severe adverse reactions have been observed in the hemopoietic system (see BOXED WARNING), the liver and the cardiovascular system.

The most frequently observed adverse reactions, particularly during the initial phases of therapy, are dizziness, drowsiness, unsteadiness, nausea, and vomiting. To minimize the possibility of such reactions, therapy should be initiated at the low dosage recommended.

The following additional adverse reactions have been reported:

Hemopoietic System: Aplastic anemia, agranulocytosis, pancytopenia, bone marrow depression, thrombocytopenia, leukopenia, leukocytosis, eosinophilia, acute intermittent porphyria.

Skin: Toxic epidermal necrolysis (TEN) and Stevens-Johnson syndrome (SJS) (see BOXED WARNING), pruritic and erythematous rashes, urticaria, photosensitivity reactions, alterations in skin pigmentation, exfoliative dermatitis, erythema multiforme and nodosum, purpura, aggravation of disseminated lupus erythematosus, alopecia, and diaphoresis. In certain cases, discontinuation of therapy may be necessary. Isolated cases of hirsutism have been reported, but a causal relationship is not clear.

Cardiovascular System: Congestive heart failure, edema, aggravation of hypertension, hypotension, syncope and collapse, aggravation of coronary artery disease, arrhythmias and AV block, thrombophlebitis, thromboembolism, and adenopathy or lymphadenopathy.

Some of these cardiovascular complications have resulted in fatalities. Myocardial infarction has been associated with other tricyclic compounds.

Liver: Abnormalities in liver function tests, cholestatic and hepatocellular jaundice, hepatitis; very rare cases of hepatic failure.

Pancreatic: Pancreatitis.

Respiratory System: Pulmonary hypersensitivity characterized by fever, dyspnea, pneumonitis, or pneumonia.

Genitourinary System: Urinary frequency, acute urinary retention, oliguria with elevated blood pressure, azotemia, renal failure, and impotence. Albuminuria, glycosuria, elevated BUN, and microscopic deposits in the urine have also been reported.

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