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
126283671 12628367 1 I 20160726 20160808 20160808 EXP IT-CIPLA LTD.-2016MW10309 CIPLA 0.00 Y 0.00000 20160808 OT IT MW

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
126283671 12628367 1 SS STAVUDINE. STAVUDINE 1 Transplacental UNK 0
126283671 12628367 2 SS STAVUDINE. STAVUDINE 1 Transmammary UNK 0
126283671 12628367 3 SS LAMIVUDINE. LAMIVUDINE 1 Transplacental UNK 0
126283671 12628367 4 SS LAMIVUDINE. LAMIVUDINE 1 Transmammary UNK 0
126283671 12628367 5 PS NEVIRAPINE. NEVIRAPINE 1 Transplacental UNK 77956
126283671 12628367 6 SS NEVIRAPINE. NEVIRAPINE 1 Transmammary UNK 77956
126283671 12628367 7 SS NEVIRAPINE. NEVIRAPINE 1 Unknown 2 MG/KG, SINGLE 77956 2 MG/KG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126283671 12628367 5 Prophylaxis against HIV infection

Outcome of event

Event ID CASEID OUTC COD
126283671 12628367 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126283671 12628367 Anaemia
126283671 12628367 Exposure during breast feeding
126283671 12628367 Foetal exposure during pregnancy

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

no results found

Therapies reported

no results found