Internal-Medicine
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268 13: Clinical Pharmacology<br />
10. (A) Folate deficiency can be secondary to small<br />
bowel disease, alcoholism, inadequate intake,<br />
disease states with high cell turnover (hemolytic<br />
anemia), drugs (methotrexate), and pregnancy.<br />
The concentration of folate in plasma changes<br />
rapidly with changes in food intake, so the<br />
diagnosis of anemia secondary to folate deficiency<br />
is made more reliable by measuring red<br />
blood cell folate. (Brunton, p. 1460)<br />
11. (D) Vitamin B 12<br />
absorption is best in the distal<br />
ileum. Receptors for the intrinsic factor are<br />
present in the distal ileum, but mass action<br />
absorption also occurs with large doses.<br />
However, the oral route is still felt to be unreliable<br />
if hematologic or neurologic effects are<br />
present. The Schilling test, with and without<br />
intrinsic factor, can help diagnose the exact<br />
cause of B 12<br />
deficiency. (Brunton, pp. 1454–1455)<br />
12. (A) Sympathomimetic effects such as pupillary<br />
dilatation, piloerection, hyperthermia, and<br />
tachycardia are common in an overdosage of<br />
LSD. Other symptoms include dizziness, weakness,<br />
drowsiness, nausea, and paresthesias. The<br />
hallucinogenic effects can last for hours and<br />
are mainly visual. (Brunton, pp. 624–625)<br />
13. (D) GI symptoms are the major side effects of<br />
tetracycline. Stomatitis, glossitis, and diarrhea<br />
are seen and may be related to superinfections.<br />
Hepatic toxicity has been reported but is rare<br />
except in massive doses or during pregnancy.<br />
Tetracyclines can cause discoloration of teeth in<br />
children and in fetuses of mothers given the<br />
drug during pregnancy. (Brunton, p. 1178)<br />
14. (D) Thrombocytopenia usually occurs after<br />
weeks or months of therapy. It is due to formation<br />
of drug-platelet complexes that evoke a<br />
circulating antibody. Thrombocytopenia and<br />
bleeding can be severe but resolve rapidly on<br />
discontinuing the drug. The antibody is longlasting,<br />
and reintroduction of quinidine, even<br />
in a small dose, can rapidly cause thrombocytopenia.<br />
Other hypersensitivity reactions to<br />
quinidine include hepatitis, bone marrow suppression,<br />
and a lupus syndrome. The most<br />
common side effects of quinidine are gastrointestinal<br />
and include nausea, vomiting, and<br />
diarrhea. (Brunton, pp. 928–929)<br />
15. (C) Lithium is used primarily for bipolar affective<br />
disorder, either to treat mania or prevent<br />
recurrences of the bipolar disorder. It has also<br />
been used in severe unipolar depression. Acute<br />
intoxication can result in vomiting, diarrhea,<br />
tremor, ataxia, coma, and convulsions. Leukocytosis<br />
is also a side effect of lithium therapy.<br />
Polyuria and polydipsia secondary to acquired<br />
nephrogenic diabetes insipidus is a common<br />
side effect. Both acute and chronic intoxication<br />
can be lethal. The toxic and therapeutic levels<br />
of lithium are very close, and patients on<br />
lithium require close medical observation,<br />
including measurement of serum lithium levels.<br />
(Brunton, pp. 487–488)<br />
16. (E) The benefit of nitroglycerin is probably due<br />
to diminution in cardiac output and work of the<br />
heart. Nitroglycerin generally dilates most veins<br />
and arteries, and this result in both a decreased<br />
preload and a decreased afterload for the heart.<br />
This leads to decreased myocardial oxygen<br />
requirements. Although coronary artery dilation<br />
also occurs, it is probably not as important in<br />
relieving anginal pain. (Brunton, pp. 827–828)<br />
17. (C) Allopurinol effectively blocks uric acid<br />
production by inhibiting xanthine oxidase.<br />
Allopurinol is indicated in patients with a<br />
history of uric acid calculi of the urinary tract.<br />
In addition, it is often used in patients with<br />
malignancy (e.g., leukemia, lymphoma), particularly<br />
when chemotherapy or radiation therapy<br />
is being used. (Brunton, pp. 708–709)<br />
18. (E) Heparin must be given parenterally (usually<br />
intravenously or subcutaneously) to be<br />
active, and its activity is monitored by the partial<br />
thromboplastin time (PTT), not the PT. It is<br />
safer than oral anticoagulants in pregnancy and<br />
does not deplete clotting factors as its mode<br />
of action. Rather, it potentiates the effect of<br />
antithrombin III on the clotting cascade. It can<br />
be neutralized by administration of protamine.<br />
Because protamine can cause a bleeding tendency<br />
by its own actions, it is used only when<br />
bleeding is severe, and in the lowest possible<br />
dose. When low-molecular weight-heparin is<br />
used, it has a more predictable pharmacokinetic<br />
profile which allows for a weight-adjusted