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
125857981 12585798 1 I 20160718 20160725 20160725 EXP ZA-STRIDES ARCOLAB LIMITED-2016SP010409 STRIDES 0.00 Y 0.00000 20160725 OT ZA ZA

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
125857981 12585798 1 PS NEVIRAPINE. NEVIRAPINE 1 Transplacental UNK 78195
125857981 12585798 2 SS NEVIRAPINE. NEVIRAPINE 1 UNK 78195

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125857981 12585798 1 Infection prophylaxis

Outcome of event

Event ID CASEID OUTC COD
125857981 12585798 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125857981 12585798 Foetal distress syndrome
125857981 12585798 Foetal exposure during pregnancy
125857981 12585798 Low birth weight baby
125857981 12585798 Neonatal asphyxia
125857981 12585798 Premature baby

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

no results found

Therapies reported

no results found