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
126283311 12628331 1 I 20160726 20160808 20160808 EXP IT-CIPLA LTD.-2016MW10307 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
126283311 12628331 1 SS STAVUDINE. STAVUDINE 1 Transplacental UNK 0
126283311 12628331 2 SS STAVUDINE. STAVUDINE 1 Transmammary UNK 0
126283311 12628331 3 SS LAMIVUDINE. LAMIVUDINE 1 Transplacental UNK 0
126283311 12628331 4 SS LAMIVUDINE. LAMIVUDINE 1 Transmammary UNK 0
126283311 12628331 5 PS NEVIRAPINE. NEVIRAPINE 1 Transplacental UNK 77956
126283311 12628331 6 SS NEVIRAPINE. NEVIRAPINE 1 Transmammary UNK 77956
126283311 12628331 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
126283311 12628331 5 Prophylaxis against HIV infection

Outcome of event

Event ID CASEID OUTC COD
126283311 12628331 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126283311 12628331 Anaemia
126283311 12628331 Exposure during breast feeding
126283311 12628331 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