Viagra:
Effects On Other Drugs
Effects of Viagra on Other Drugs
In vitro studies:
Sildenafil
is a weak inhibitor of the cytochrome P450 isoforms 1A2, 2C9,
2C19,
2D6, 2E1 and 3A4 (IC50 >150 mM). Given sildenafil peak plasma
concentrations of
approximately 1 mM after recommended doses, it is unlikely that
Viagra will alter the clearance
of substrates of these isoenzymes.
In
vivo studies: When Viagra 100 mg oral was coadministered with
amlodipine, 5 mg or 10 mg oral, to hypertensive patients, the mean
additional reduction on supine blood pressure was 8 mmHg systolic
and 7 mmHg diastolic.
No significant interactions were shown with tolbutamide (250 mg)
or warfarin (40 mg), both of
which are metabolized by CYP2C9.
Viagra (50 mg) did not potentiate the increase in bleeding time
caused by aspirin (150 mg).
Viagra (50 mg) did not potentiate the hypotensive effect of alcohol
in healthy volunteers with
mean maximum blood alcohol levels of 0.08%.
Carcinogenesis, Mutagenesis, Impairment of Fertility
Sildenafil was not carcinogenic when administered to rats for
24 months at a dose resulting in
total systemic drug exposure (AUCs) for unbound sildenafil and
its major metabolite of 29- and
42-times, for male and female rats, respectively, the exposures
observed in human males given the
Maximum Recommended Human Dose (MRHD) of 100 mg.
Sildenafil
was not carcinogenic
when administered to mice for 18-21 months at dosages up to the
Maximum Tolerated Dose
(MTD) of 10 mg/kg/day, approximately 0.6 times the MRHD on a
mg/m2 basis. Sildenafil was negative in in vitro bacterial and Chinese hamster
ovary cell assays to detect
mutagenicity, and in vitro human lymphocytes and in vivo mouse
micronucleus assays to detect
clastogenicity.
There was no impairment of fertility in rats given sildenafil
up to 60 mg/kg/day for 36 days to
females and 102 days to males, a dose producing an AUC value of
more than 25 times the human
male AUC.
There was no effect on sperm motility or morphology after single
100 mg oral doses of Viagra
in healthy volunteers.
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