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. 2016 Sep;41(5):437–445.

Table 1.

Food and Drug Administration’s classification of selected anti-glaucoma medications and potential side effects in pregnancy

FDA’s classification Reported effect in animal studies Reports of side effects in human studies
Preservative of medications, BAK C* Doserelated increase in fetal resorption and death and minor sternal defects14
Betablockers C A case with cardiac conduction disorder. Arrhythmia and bradycardia (resolved after stopping the drug)15 Systemic use: Intrauterine growth restriction and persistent betablockade in the newborn Impairment of respiratory control in the neonate, lethargy and confusion16,17
Carbonic anhydrase Inhibitors
Oral C Forelimb anomalies18 Single case of sacrococcygealteratoma (has not been substantiated by others)19
Topical C Fetal vertebral body malformations and decrease fetal weights (dose 31 times)20,21
Prostaglandin analogs
Latanoprost C Dead fetus (dose 80 times)22 A case of miscarriage in a 46 yearold woman that seems to be due to her reproductive risk related to her advance age, not the drug23
Travoprost C Teratogen (dose 250 times)24
Bimatoprost C Reduced duration of gestation and increased incidence of dead fetus (dose 41 times)25
Parasympathomimetics
Pilocarpine C Teratogen26 Signs mimicking meningitis in the newborn27
Echothiophate iodide Suppression of the infant’s pseudocholinesterase
Sympathomimetic
Nonselective B** Congenital cataract2 Systemic: Delays the second stage of labor or cause a prolonged period of uterine atony with hemorrhage Topical: Local side effects and a high rate of systemic side effects28
Brimonidine B No fetal damage29 In infants has central nervous system effects30
Fixedcombination Antiglaucoma Medications C
FixedCombination Timolol/dorzolamide C31 As each component of the drug
FixedCombination Timolol/brimonidine C32 As each component of the drug
*

Uncertain safety, with no human studies and animal studies showing adverse effect;

**

Presumed safety based on animal studies