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
125467301 12546730 1 I 201604 20160418 20160711 20160711 EXP GB-JNJFOC-20160418545 JANSSEN 35.54 YR A M Y 0.00000 20160711 OT GB GB

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
125467301 12546730 1 PS SIMPONI GOLIMUMAB 1 Subcutaneous N UNKNOWN 125289 50 MG SOLUTION FOR INJECTION /month
125467301 12546730 2 SS RAMIPRIL. RAMIPRIL 1 Unknown U 0 UNSPECIFIED
125467301 12546730 3 C METHOTREXATE. METHOTREXATE 1 Unknown 0 20 MG UNSPECIFIED
125467301 12546730 4 C FOLIC ACID. FOLIC ACID 1 Unknown 0 5 MG UNSPECIFIED
125467301 12546730 5 C DICLOFENAC DICLOFENAC 1 Unknown 0 50 MG UNSPECIFIED
125467301 12546730 6 C OMEPRAZOLE. OMEPRAZOLE 1 Unknown 0 UNSPECIFIED
125467301 12546730 7 C CETRIZINE CETIRIZINE HYDROCHLORIDE 1 Unknown 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125467301 12546730 1 Psoriatic arthropathy
125467301 12546730 2 Hypertension
125467301 12546730 3 Psoriatic arthropathy
125467301 12546730 5 Pain
125467301 12546730 7 Seasonal allergy

Outcome of event

Event ID CASEID OUTC COD
125467301 12546730 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125467301 12546730 Adenovirus infection
125467301 12546730 Cough
125467301 12546730 Fatigue
125467301 12546730 Hyperkalaemia
125467301 12546730 Influenza like illness

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
125467301 12546730 1 201603 0
125467301 12546730 3 20110310 0
125467301 12546730 4 20110310 0