The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
126235161 12623516 1 I 20160726 20160804 20160804 EXP DE-TEVA-680224GER TEVA 0.00 YR F Y 3.07000 KG 20160805 MD DE DE

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
126235161 12623516 1 PS CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Transplacental 20 MILLIGRAM DAILY; U 77232 20 MG QD
126235161 12623516 2 C DIMENHYDRINATE. DIMENHYDRINATE 1 Transplacental 200 MILLIGRAM DAILY; U 0 50 MG QID
126235161 12623516 3 C OMEPRAZOLE. OMEPRAZOLE 1 Transplacental 20 MILLIGRAM PER DAY, IF REQUIRED U 0
126235161 12623516 4 C rennie MAGNESIUM CARBONATE 1 Transplacental SIX TIMES PER DAY U 0
126235161 12623516 5 C Folio FOLIC ACID 1 Transplacental .4 MILLIGRAM DAILY; U 0 .4 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126235161 12623516 1 Depression
126235161 12623516 2 Vomiting in pregnancy
126235161 12623516 3 Dyspepsia
126235161 12623516 4 Dyspepsia
126235161 12623516 5 Prophylaxis of neural tube defect

Outcome of event

Event ID CASEID OUTC COD
126235161 12623516 CA

Reactions reported

Event ID CASEID DRUG REC ACT PT
126235161 12623516 Aortic valve incompetence
126235161 12623516 Dysmorphism
126235161 12623516 Foetal exposure during pregnancy
126235161 12623516 Presbyacusis
126235161 12623516 Ventricular septal defect

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126235161 12623516 5 20141217 20150821 0