The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
6537768 7465947 I 6537768-4 20091229 20100111 EXP B0623717A GLAXOSMITHKLINE 49 YR M N 20100107 MD FRANCE

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
6537768 1012943675 PS LAMIVUDINE 2 D 20564
6537768 1012992592 SS FOSAMPRENAVIR 2 D
6537768 1012992595 SS TENOFOVIR 2 D
6537768 1012992600 SS RITONAVIR 1 D

Indications of drugs used

Event ID DRUG SEQ INDI PT
6537768 1012943675 HIV INFECTION
6537768 1012992592 HIV INFECTION
6537768 1012992595 HIV INFECTION
6537768 1012992600 HIV INFECTION

Outcome of event

Event ID OUTC COD
6537768 HO

Reactions reported

Event ID PT
6537768 ARTHRITIS
6537768 DRUG INEFFECTIVE
6537768 FOLLICULITIS
6537768 IMMUNE RECONSTITUTION SYNDROME
6537768 OEDEMA PERIPHERAL
6537768 PAIN IN EXTREMITY

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

Event ID RPSR COD
6537768 FGN
6537768 HP
6537768 LIT

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6537768 1012943675 20060801
6537768 1012992592 20060801
6537768 1012992595 20060801
6537768 1012992600 20060801