what is anadrol


Infection of the big toe is usually sufficient 3-month course of treatment. Some patients who have lowered the rate of nail growth may need longer treatment. Fungal infections of the skin: the duration of treatment with interdigital, plantar or “sock” type of localization of infection is 2-6 weeks, with mycoses of other parts of the body: the shins – 2 -4 weeks, the body – 2-4 weeks; in mycosis caused by fungi what is anadrol of the genus Candida – 2-4 weeks; with mycosis of the scalp, caused by fungi of the genus by Microsporum – more than 4 weeks. Babies: Typically prescribed 125 mg. When the body weight of 20 to 40 kg – 125 mg 1 time per day. With a body weight over 40 kg – 250 mg 1 time . day duration of treatment of fungal infections of the scalp is approximately 4 weeks after infection Microsporum canis – maybe longer. Older patients the drug is administered in the same dose as adults. patients with hepatic and renal insufficiency administered at a dose of 125 1 mg once a day.


ADVERSE EFFECTS From the digestive tract: often: the feeling of fullness, nausea, abdominal pain, diarrhea, loss of appetite; in a few cases (0.1-1%) – taste disturbance, including their loss (recovery occurs within a few weeks after cessation of treatment); rarely (0.01-0.1%) – hepatotoxic effects (increased activity what is anadrol of “liver” enzymes, liver failure). On the part of the central nervous system: common: headache, dizziness. From the hematopoietic system: very rarely (<0, 01%), neutropenia, agranulocytosis, thrombocytopenia. immune system: rare: anaphylactoid reactions, including angioedema, exacerbation of systemic lupus erythematosus. skin and subcutaneous tissue: common: rash, urticaria; very rare: psoriasiform rashes on the skin, exacerbation of psoriasis, Stevens-Johnson syndrome, toxic epidermal necrolysis, hair loss, acute generalized exanthematous pustulosis. On the part of the musculoskeletal system and connective tissue disorders: common: arthralgia, myalgia. General disorders: very rare: fatigue.


Interaction with other drugs
inhibits the CYP2D6 isoenzyme and disrupts the metabolism of drugs such as tricyclic antidepressants and selective serotonin reuptake inhibitors (eg desipramine, fluvoxamine), β-blockers (metoprolol, propranolol), antiarrhythmics (flecainide, propafenone), monoamine oxidase inhibitors The type (e.g., selegiline) and antipsychotic (e.g., chlorpromazine, haloperidol) means.
drugs – cytochrome what is anadrol isoenzyme inducers (e.g. rifampicin) can accelerate the metabolism and excretion of the organism terbinafine. Drugs – inhibitors of cytochrome P450 isoenzymes (eg, cimetidine) may slow the metabolism and excretion of terbinafine from the body. With the simultaneous use of these drugs may require adjustment of the dose of terbinafine.
Perhaps the menstrual cycle while taking terbinafine and oral contraceptives.
Terbinafine decreases the clearance of caffeine by 19% and prolongs its half-life by 31%. It does not affect the clearance of phenazone, digoxin, warfarin.
When combined with ethanol what is anadrol or drugs having gepatoksicheskim action, there is the risk of liver disease drug.