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
125270362 12527036 2 F 20141112 20160718 20160705 20160721 EXP US-GLAXOSMITHKLINE-US2016094327 GLAXOSMITHKLINE 57.00 YR F Y 0.00000 20160721 CN US US

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
125270362 12527036 1 PS VOLTAREN DICLOFENAC SODIUM 1 UNK W0182 22122 GEL

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125270362 12527036 1 Osteoarthritis

Outcome of event

Event ID CASEID OUTC COD
125270362 12527036 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125270362 12527036 Ankle fracture
125270362 12527036 Application site hypoaesthesia
125270362 12527036 Arthralgia
125270362 12527036 Arthritis
125270362 12527036 Drug administered at inappropriate site
125270362 12527036 Expired product administered
125270362 12527036 Fall
125270362 12527036 Hypoaesthesia
125270362 12527036 Infection
125270362 12527036 Osteoarthritis
125270362 12527036 Pain
125270362 12527036 Rheumatoid arthritis

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
125270362 12527036 1 2012 0