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
125832691 12583269 1 I 201602 20160719 20160722 20160722 EXP US-GLAXOSMITHKLINE-US2016104759 GLAXOSMITHKLINE 71.00 YR F Y 0.00000 20160722 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
125832691 12583269 1 PS VOLTAREN DICLOFENAC SODIUM 1 UNK W5558 22122 GEL
125832691 12583269 2 SS VOLTAREN DICLOFENAC SODIUM 1 22122 GEL
125832691 12583269 3 SS VOLTAREN DICLOFENAC SODIUM 1 22122 GEL

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125832691 12583269 1 Arthritis
125832691 12583269 2 Musculoskeletal pain
125832691 12583269 3 Back pain

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125832691 12583269 Arthritis
125832691 12583269 Back pain
125832691 12583269 Drug administered at inappropriate site
125832691 12583269 Drug ineffective
125832691 12583269 Intentional product misuse
125832691 12583269 Musculoskeletal pain
125832691 12583269 Therapeutic response unexpected

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
125832691 12583269 1 2015 0