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
127162311 12716231 1 I 200208 20021028 20160906 20160906 EXP FR-BRISTOL-MYERS SQUIBB COMPANY-12095063 BRISTOL MYERS SQUIBB 32.00 YR F Y 0.00000 20160906 CN FR FR

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
127162311 12716231 1 PS SUSTIVA EFAVIRENZ 1 Oral 600 MG, QD Y 20972 600 MG CAPSULE QD
127162311 12716231 2 C COMBIVIR LAMIVUDINEIDOVUDINE 1 Unknown 300/150 U 0 1 DF

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127162311 12716231 1 HIV infection
127162311 12716231 2 Antiretroviral therapy

Outcome of event

Event ID CASEID OUTC COD
127162311 12716231 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127162311 12716231 Abortion induced
127162311 12716231 Abortion spontaneous
127162311 12716231 Maternal exposure during pregnancy
127162311 12716231 Twin pregnancy
127162311 12716231 Vanishing twin syndrome

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
127162311 12716231 1 20020831 0