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
97682703 9768270 3 F 20150429 20131217 20160714 EXP GB-BRISTOL-MYERS SQUIBB COMPANY-19923655 BRISTOL MYERS SQUIBB 39.00 YR F Y 0.00000 20160714 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
97682703 9768270 1 PS TRIAMCINOLONE ACETONIDE. TRIAMCINOLONE ACETONIDE 1 Intra-arterial 40 MG, UNK U 12041 40 MG SUSPENSION FOR INJECTION
97682703 9768270 2 I RITONAVIR. RITONAVIR 1 Unknown U 0
97682703 9768270 3 C DARUNAVIR DARUNAVIR 1 Unknown U 0
97682703 9768270 4 C EMTRICITABINE / TENOFOVIR DISOPROXIL FUMARATE EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
97682703 9768270 1 Product used for unknown indication
97682703 9768270 2 Antiretroviral therapy
97682703 9768270 3 Antiretroviral therapy
97682703 9768270 4 Antiretroviral therapy

Outcome of event

Event ID CASEID OUTC COD
97682703 9768270 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
97682703 9768270 Adrenal suppression
97682703 9768270 Cushing's syndrome
97682703 9768270 Drug interaction

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

no results found

Therapies reported

no results found