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
123606162 12360616 2 F 201604 20160721 20160512 20160729 EXP BR-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-036406 BRISTOL MYERS SQUIBB 51.13 YR F Y 0.00000 20160729 CN BR BR

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
123606162 12360616 1 PS ABATACEPT ABATACEPT 1 Intravenous (not otherwise specified) 750 MG, QMO Y 125118 750 MG SOLUTION FOR INFUSION /month
123606162 12360616 2 SS ACLASTA ZOLEDRONIC ACID 1 Unknown UNK U U 0
123606162 12360616 3 C GLIFAGE METFORMIN HYDROCHLORIDE 1 Unknown U 0
123606162 12360616 4 C PREDNISONE. PREDNISONE 1 Unknown U 0
123606162 12360616 5 C PIROXICAM. PIROXICAM 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123606162 12360616 1 Rheumatoid arthritis
123606162 12360616 2 Product used for unknown indication
123606162 12360616 3 Product used for unknown indication
123606162 12360616 4 Product used for unknown indication
123606162 12360616 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123606162 12360616 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123606162 12360616 Abdominal pain
123606162 12360616 Arthritis
123606162 12360616 Back pain
123606162 12360616 Diabetes mellitus
123606162 12360616 Hypersensitivity
123606162 12360616 Nausea
123606162 12360616 Pyrexia

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

no results found

Therapies reported

no results found