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
125872651 12587265 1 I 20160718 20160725 20160725 EXP ZA-STRIDES ARCOLAB LIMITED-2016SP010416 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
125872651 12587265 1 PS NEVIRAPINE. NEVIRAPINE 1 Transplacental UNK 78195
125872651 12587265 2 SS NEVIRAPINE. NEVIRAPINE 1 UNK 78195

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125872651 12587265 1 Infection prophylaxis

Outcome of event

Event ID CASEID OUTC COD
125872651 12587265 OT
125872651 12587265 CA

Reactions reported

Event ID CASEID DRUG REC ACT PT
125872651 12587265 Congenital pneumonia
125872651 12587265 Foetal distress syndrome
125872651 12587265 Foetal exposure during pregnancy
125872651 12587265 Low birth weight baby
125872651 12587265 Premature baby

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

no results found

Therapies reported

no results found