DRUGS BRJ3GNANCY VIRGINIA GAR Since the thalidomide tragedy of 1960 to 1962, pregnant women have been in a quandry about taking com- mon medications on their own in- itiative, and physicians have been troubled about prescribing drugs for them. Peckham and King have shown recently that 92 percent of women have at least one drug prescribed by their physicians during pregnancy, and 3.9 percent are given 10 or more ( 1). There is no count of babies who have survived because of drugs ad- ministered during pregnancy, infants who escaped birth defects because their mothers were given certain drugs, or full-tern babies who might have been born prematurely without drugs. Both physicians and patients rightly demand to know what infor- mation is available about drugs and human pregnancy. Very little is known that can actu- ally be applied to all pregnancies. According to Lenz, 80 percent of the mothers who took thalidomide dur- ing the period of fetal sensitivity had normal infants (2). What was it in the genetic background of the mother or the father that caused the serious anomalies that occurred in 20 per- cent of the infants? What environ- mental associations were related? The answers to these questions are a long way off. This past year, two useful reviews appeared, by Cohlan and Lucey, about the effect of medication ad- ministered during pregnancy on the fetus and newborn infant, from which these comments are largely drawn (3,4). Two other reviews, which dis- cuss in detail the problems of human teratogenesis, were written by Wark- any and Kalter and by Fraser. All are ~ DR. AF'GAR is o member of the pediatrics panel of the hrican Medical Association Registry on Ad\lase Reactions. highly recommended (5,6). The table lists some relationships observed between maternal medica- tion and fetal or neonatal changes. Only a few are proved beyond a shad- OW of doubt, but until further data are collected, caution should be exer- cised in administering these sub- stances to pregnant women. The best way to determine a post hoc ergo propter hoc relationship between maternal medication and changes in the fetus and newborn infant is to conduct a prospective study in a population of women who enter the study by the eighth week of pregnancy. They shdd be frequent- ly observed and interrogated by only one, two, or three astute clinicians, and the data should be entered and analyzed within a few hours' time. Such a study, a continuation of the Fetal Life Study of McIntosh and Menitt begun in 1947, is being con- ducted by Mellin (8). Routine ques- tioning about the intake of certain drugs formed the basis of their re- port that meclizine hydrochloride ( Bonadettes, Bonine Hydrochloride) was not under suspicion as a terato- genic agent (9). Other prospective studies, such as that of the Kaiser Permanente group, and the Collabo- rative Study of the National Institute of Neurological Disease and Blind- ness can be expected to show certain relationships between medication ad- ministered during pregnancy and fe- tal and neonatal changes. But these studies lack the accuracy achieved by a small, closely controlled group of pregnant women, observed by the same professional team. The greatest danger of inducing malformations is in the first trimester of pregnancy. Since this includes the period before a woman may be aware that she is pregnant, and since we know very little about the effects of drugs on the fetus, physicians are AMERICAN JOURNAL OF NURSING MEDICATION AND CHANGES PRODUCED FETAL OR NEONATAL EFFECT MATERNAL MEDICATION Oral progestogens Androgens Estrogens Cortisone Acetate (Cortogen Acetate, Cortone Acetate) Potassium iodide Ropylthiouracil Methimazole (Tapazole) lophenoxic acid (`reridax) Sodium aminopterin Methotrexate (Amethopterin) Chlorambucil (Leukeran) Bishydroxyeoumarin (Dicumrd) Ethyl bicoumacetate (Tromexan Ethyl Acetate) Sodium warfarin (Coumadin Sodium. Panwadin, Prothromadin) Salicylates (large amounts) Streptomycin Sulfonamides Chloramphenicol (Chloromycetin) Sodium novobiocin (Albamycin Sodium. Cathomycin Sodium) Erythromycin (Ilwone) Nitrofurantoin (Furadantin) Tetracyclines Vitamin K Analogues (in excess) Ammonium chloride Intravenous fluids (in ~xcSS) Reserpine (Rauloydin. Raurine. ~au-sod, Reserpoid. Sandril. Serfin. Serpasil. Serpate. VleSerpine) Hexamethonium bromide (Birtrium Bromide) Herdn and morphine phenobarbital Qn axcast) Smoking Sulphonylurea derivatives phenformin hydrochloride (DBI) phenothlulnes MoprobanutO (Equanll. weals. Mwrormn. Meprotab ,MlWn) .- _: . chloruqulrhe phosphate (Anlen I. ,PhOa*tO) minlno -- ThaIMomlde . V~IUUO~. imailpox V.cclnaUon. Influenza Antihlstamlnes Thlulde dluretlcs Masculinization and advanced bone age Anomalies: cleft palate (1) Goiter and mental retardation Elevation of P.B.I. Anomalies and abortion Fetal death; hemorrhage Neonatal bleeding Possible 8th nerve deafness Kernicterus "Grey" syndrome: death Hyperbilirubinemia Uver damage (?I Hemolysis I Inhibition of bone growth Discoloration of teeth Hyperbilirubinemia Acidosis Electrolyte Abnormalities Stuffy nose: respiratory obstruction Neonatal ileus Neonatal death Neonatal bleeding: death Birth of small babies Anomalies Cn Lactic acidosis 0 Hyperbilimblnemia (?I ~etaded development 0 Retinal damage or death 0 Thrybocytopenia .. phocomelia: death; hearing 1- Fetal vaccinia i&a~d antiA ad B titers in mothers ~nmiies (?I: Infedlity Cn Thrombocytopenia 0) -