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
126184321 12618432 1 I 20160723 20160728 20160803 20160803 EXP US-GLAXOSMITHKLINE-US2016111421 GLAXOSMITHKLINE 57.00 YR F Y 0.00000 20160803 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
126184321 12618432 1 PS VOLTAREN DICLOFENAC SODIUM 1 UNK Y W5855 22122 GEL

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126184321 12618432 1 Bone pain

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126184321 12618432 Abdominal pain upper
126184321 12618432 Cough
126184321 12618432 Diarrhoea
126184321 12618432 Formication
126184321 12618432 Inappropriate schedule of drug administration
126184321 12618432 Influenza like illness
126184321 12618432 Intentional product misuse
126184321 12618432 Pain
126184321 12618432 Pruritus generalised
126184321 12618432 Vomiting
126184321 12618432 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

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126184321 12618432 1 20160722 20160725 0