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
126367541 12636754 1 I 20160726 20160809 20160809 EXP IT-CIPLA LTD.-2016MW10255 CIPLA 0.00 Y 0.00000 20160809 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
126367541 12636754 1 SS ZIDOVUDINE. ZIDOVUDINE 1 Unknown 300 MG, BID STARTING FROM WEEK 25 OF GESTATIONAL AGE UNTIL 6 MONTHS POSTPARTUM U U 0 300 MG BID
126367541 12636754 2 SS ZIDOVUDINE. ZIDOVUDINE 1 Unknown UNK, 3 WEEK TAIL U U 0
126367541 12636754 3 SS LAMIVUDINE. LAMIVUDINE 1 Unknown 150 MG, BID STARTING FROM WEEK 25 OF GESTATIONAL AGE UNTIL 6 MONTHS POSTPARTUM U U 0 150 MG BID
126367541 12636754 4 SS LAMIVUDINE. LAMIVUDINE 1 Unknown UNK, 3 WEEK TAIL U U 0
126367541 12636754 5 PS NEVIRAPINE. NEVIRAPINE 1 Unknown 200 MG, QD FOR FIRST 14 DAYS OF TREATMENT U U 77956 200 MG QD
126367541 12636754 6 SS NEVIRAPINE. NEVIRAPINE 1 Unknown 200 MG, BID, THEREAFTER, STARTING FROM WEEK 25 OF GESTATIONAL AGE UNTIL 6 MONTHS POSTPARTUM U U 77956 200 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126367541 12636754 1 Prophylaxis against HIV infection
126367541 12636754 3 Prophylaxis against HIV infection
126367541 12636754 5 Prophylaxis against HIV infection

Outcome of event

Event ID CASEID OUTC COD
126367541 12636754 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126367541 12636754 Drug resistance
126367541 12636754 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