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
125698961 12569896 1 I 20160713 20160713 20160719 20160719 EXP US-GLAXOSMITHKLINE-US2016101927 GLAXOSMITHKLINE 0.00 F Y 0.00000 20160719 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
125698961 12569896 1 PS VOLTAREN DICLOFENAC SODIUM 1 Topical UNK UNK 22122 GEL
125698961 12569896 2 SS VOLTAREN DICLOFENAC SODIUM 1 22122 GEL
125698961 12569896 3 SS VOLTAREN DICLOFENAC SODIUM 1 22122 GEL

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125698961 12569896 1 Joint arthroplasty
125698961 12569896 2 Arthropathy
125698961 12569896 3 Arthralgia

Outcome of event

Event ID CASEID OUTC COD
125698961 12569896 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125698961 12569896 Bronchitis
125698961 12569896 Fall
125698961 12569896 Joint injury
125698961 12569896 Malaise
125698961 12569896 Off label use
125698961 12569896 Osteoporosis
125698961 12569896 Upper limb fracture

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

no results found

Therapies reported

no results found