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
127362211 12736221 1 I 20160830 20160913 20160913 EXP GB-AUROBINDO-AUR-APL-2016-11135 AUROBINDO 33.00 YR F Y 82.00000 KG 20160913 OT GB GB

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
127362211 12736221 1 PS NEVIRAPINE. NEVIRAPINE 1 Oral 400 MG, ONCE A DAY 77521 400 MG QD
127362211 12736221 2 SS RETROVIR ZIDOVUDINE 1 Oral 500 MG, ONCE A DAY 0 500 MG QD
127362211 12736221 3 SS VIDEX DIDANOSINE 1 Oral 400 MG, ONCE A DAY 0 400 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127362211 12736221 1 HIV infection
127362211 12736221 2 HIV infection
127362211 12736221 3 HIV infection

Outcome of event

Event ID CASEID OUTC COD
127362211 12736221 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127362211 12736221 Exposure during pregnancy
127362211 12736221 Pregnancy
127362211 12736221 Stillbirth

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
127362211 12736221 1 20000122 0
127362211 12736221 2 200001 0
127362211 12736221 3 20040122 0