The Safety Rates Drug Report

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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
127027731 12702773 1 I 20160627 20160818 20160831 20160831 EXP DE-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-122838 RANBAXY 1.00 DY M Y 3.70000 KG 20160831 OT 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
127027731 12702773 1 PS SERTRALINE SERTRALINE HYDROCHLORIDE 1 Transplacental 100 [MG/D (50MG)]/SINCE 13.05.2016: 100 MG SERTRALINE; 0.38.2 GW U U 77977
127027731 12702773 2 SS DIAZEPAM. DIAZEPAM 1 Transplacental 8 [MG/D (-6 MG/D)]/FROM 28.04 UNTIL 26.05.2016: 8 MG/D; WEEK 37+2 UNTIL DELIVERY 3 X 2 MG/D; 0.-38.2 U U 0
127027731 12702773 3 C Femibion (NEM) 2 Transplacental 1.5-38.2 GESTATIONAL WEEK U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127027731 12702773 1 Depression
127027731 12702773 2 Depression
127027731 12702773 3 Prophylaxis of neural tube defect

Outcome of event

Event ID CASEID OUTC COD
127027731 12702773 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127027731 12702773 Atrial septal defect
127027731 12702773 Drug withdrawal syndrome neonatal
127027731 12702773 Respiratory disorder neonatal

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
127027731 12702773 1 20151003 20160627 0
127027731 12702773 2 20151003 20160627 0
127027731 12702773 3 20151015 20160627 0