The FDA's pregnancy safety designation of Category A for a drug means:
A) no adequate animal studies or adequate studies of pregnant women have been done.
B) animal studies have demonstrated adverse effects, but there are no adequate studies in pregnant women; benefits may be acceptable despite the potential risks.
C) adequate studies in pregnant women have not demonstrated a risk to the fetus in the first trimester or later trimesters.
D) fetal risk has been demonstrated, which outweighs any possible benefit to the mother; avoid using in pregnant or potentially pregnant patients.
Question 2
A patient informs you that he has had his gallbladder surgically removed. Based on the physiology of the gallbladder, which one of the following is true?
A) He may have difficulty digesting large amounts of fats.
B) He cannot store glycogen produced by the liver.
C) He will be more prone to gastric ulcers.
D) He must avoid meals high in complex carbohydrates.
) Subcutaneous drug administration: (b) the administration site is prepped
) Intramuscular drug administration: (d) the needle is removed and the puncture site is covered wi
Becoming a biped changes the way an animal balances.
Drug Administration Guidelines with Enteral Feedings
Rating of Drug Interactions
Does pregnancy occur during breastfeeding? "هل يحدث حمل أثناء الرضاعة