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
126270021 12627002 1 I 20160716 20160726 20160805 20160805 EXP GB-MHRA-EYC 00142729 GB-TEVA-681627ACC TEVA 74.00 YR M Y 81.00000 KG 20160805 CN 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
126270021 12627002 1 PS ATORVASTATIN ATORVASTATIN 1 N U 02752 78773 20 MG
126270021 12627002 2 C RAMIPRIL. RAMIPRIL 1 0
126270021 12627002 3 C WARFARIN WARFARIN 1 0
126270021 12627002 4 C FINASTERIDE. FINASTERIDE 1 0
126270021 12627002 5 C ALFUZOSIN ALFUZOSIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126270021 12627002 1 Blood cholesterol increased

Outcome of event

Event ID CASEID OUTC COD
126270021 12627002 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126270021 12627002 Cardiac fibrillation
126270021 12627002 Lymphadenopathy
126270021 12627002 Pain in extremity

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
126270021 12627002 1 20160714 20160717 0