There are a lot of
physiologic changes in pregnancy that can significantly alter
the bio-availability of drugs taken orally. A higher dose is
generally needed for pregnant patients with a few exceptions. Monitoring of
doses is very important to make sure that there is no adverse effect to the
mother and the fetus. Birth defects are the most common adverse effect of
irresponsible drug consumption.
Contraindicated
drugs
Abuse of these drugs
may have teratogenic effects.
- Erythromycin can cause acute cholestatic hepatitis in pregnant mother.
- Metronidazole can cause mutation in the fetus.
- Aminoglycosides can cause ototoxicity and ear problems.
- Warfarin can result in facial dimorphism, nasal hypoplasia and defective bone mineralization in the fetus.
- ACE inhibitors can cause renal dysgenesis in the fetus.
- Live vaccines such as chicken pox, MMR and polio can cause vertical transmission to the fetus.
FDA
Classification
The Food and Drug
Administration (FDA) classify drugs as A, B and X, based on the drug safety for
use in pregnancy.
Category A- these drugs demonstrated no fetal risk
during controlled trials.
Category B- these drugs show no evidence of risk
although they should be consulted with a doctor before consumption as abuser
may have severe adverse effects.
Category X drugs- these drugs are absolutely
contraindicated in pregnancy due to proven fetal risk.
Assessment of risk
versus benefit is the main rule in drug prescribing for pregnant patients. Drug
therapy should only be given when necessary, with the lowest possible dose and
shortest possible duration, without compromising its therapeutic effect and the
final decision should be made by a physician.
No comments:
Post a Comment