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
126934442 12693444 2 F 2013 20160920 20160829 20160923 EXP US-GLAXOSMITHKLINE-US2016124479 GLAXOSMITHKLINE 82.00 YR F Y 0.00000 20160923 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
126934442 12693444 1 PS VOLTAREN DICLOFENAC SODIUM 1 UNK UNK 22122 GEL
126934442 12693444 2 SS VOLTAREN DICLOFENAC SODIUM 1 22122 GEL

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126934442 12693444 1 Back pain
126934442 12693444 2 Musculoskeletal discomfort

Outcome of event

Event ID CASEID OUTC COD
126934442 12693444 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126934442 12693444 Application site paraesthesia
126934442 12693444 Arthralgia
126934442 12693444 Back pain
126934442 12693444 Drug administered at inappropriate site
126934442 12693444 Intentional product misuse
126934442 12693444 Musculoskeletal discomfort
126934442 12693444 Pain in extremity
126934442 12693444 Wrong technique in product usage process

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

no results found

Therapies reported

no results found