Minoxidil
Minoxidil is an efficacious antihypertensive in patients
with drug-resistant, severe hypertension. It acts through an active metabolite
minoxidil N-O sulfate, which produces arteri-olar vasodilatation (without
effect on capacitance vessels). Minoxidil increases blood flow to skin,
skeletal muscle, GI tract, and heart. Apart from its use in hypertension,
minoxidil is also used topically to promote hair growth in patients with male
pattern baldness.
About 95% bioavailability; protein binding is not
significant; volume of distribution is 2 to 3 L/kg; elimination half-life
varies from 2.3 to 28.9 hours.
· Pericardial effusion, pulmonary
hypertension, dermatitis, breast tenderness or gynaecomastia, oedema, pulse and
BP changes, shortness of breath, dizziness, headache, redness of conjunctivae,
and increased growth of facial, and (later) body hair. Some of these effects
appear even on topical application.
·
Several cases of allergic contact dermatitis have been
reported when minoxidil has been used in the treatment of baldness.
·
There have also been several case reports of women applying
5% topical minoxidil, over a period of 2 to 3 months, to treat androgenetic
alopecia and subsequently developing severe hypertrichosis of the face and
extremities. The excessive hair growth on the face and limbs gradually
disappeared over a period of several months after discontinuation of minoxidil.
·
Moderate to severe hypotension.
·
Angina pectoris and haemorrhagic
pericarditis have also been reported after minoxidil overdose.
·
Coma can occur.
In
treating hypotension due to minoxidil, avoid cardiac stimu-lating sympathomimetics
such as adrenaline and noradrena-line. When a vital organ is underperfused, use
phenylephrine, vasopressin, dopamine, or angiotensin II. Haemodialysis may be
useful in minoxidil overdose.
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