Several recent epidemiologic studies suggest a positive statistical association between ssri use including celexa in pregnancy and pphn.
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Table 3 enumerates the incidencerounded to the nearest percentof treatment-emergent adverse events that occurred among 1063 depressed patients who received Celexa at doses ranging from 10 to 80 mg/day in placebo-controlled trials of up to 6 weeks in durationEvents included are those occurring in 2or more of patients treated with Celexa and for which the incidence in patients treated with Celexa was greater than the incidence in placebo-treated patients.
The prescriber should be aware that these figures cannot be used to predict the incidence of adverse events in the course of usual medical practice where patient characteristics and other factors differ from those which prevailed in the clinical trialsSimilarlythe cited frequencies cannot be compared with figures obtained from other clinical investigations involving different treatmentsusesand investigatorsThe cited figureshoweverdo provide the prescribing physician with some basis for estimating the relative contribution of drug and non-drug factors to the adverse event incidence rate in the population studied.
This medication may interfere with certain medical/laboratory testsincluding brain scan for Parkinson’s diseasepossibly causing false test resultsMake sure laboratory personnel and all your doctors know you use this drug.
Measure liquid medicine with the dosing syringe providedor with a special dose-measuring spoon or medicine cupIf you do not have a dose-measuring deviceask your pharmacist for one.
Children may be more sensitive to the side effects of this drugespecially loss of appetite and weight lossMonitor weight and height in children who are taking this drug.
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