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
74083925 7408392 5 F 20100421 20160824 20100603 20160824 EXP FR-BRISTOL-MYERS SQUIBB COMPANY-15126741 BRISTOL MYERS SQUIBB 31.00 YR F Y 0.00000 20160824 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
74083925 7408392 1 PS SUSTIVA EFAVIRENZ 1 Oral 600 MG, QD Y 20972 600 MG CAPSULE QD
74083925 7408392 2 SS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Unknown UNK U 0
74083925 7408392 3 SS KALETRA LOPINAVIRRITONAVIR 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
74083925 7408392 1 HIV infection
74083925 7408392 2 HIV infection
74083925 7408392 3 HIV infection

Outcome of event

Event ID CASEID OUTC COD
74083925 7408392 OT
74083925 7408392 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
74083925 7408392 Abortion induced
74083925 7408392 Bartholinitis
74083925 7408392 Maternal exposure during pregnancy
74083925 7408392 Pyelonephritis

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
74083925 7408392 1 20070817 20091202 0
74083925 7408392 2 20070817 0