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
125542061 12554206 1 I 20160616 20160630 20160713 20160713 EXP GB-MHRA-EYC 00141594 GB-TEVA-674225ACC TEVA 66.00 YR M Y 69.70000 KG 20160713 MD 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
125542061 12554206 1 PS OLANZAPINE. OLANZAPINE 1 Oral N U 76000 10 MG
125542061 12554206 2 C AMLODIPINE AMLODIPINE BESYLATE 1 0
125542061 12554206 3 C ASPIRIN. ASPIRIN 1 0
125542061 12554206 4 C ATORVASTATIN ATORVASTATIN 1 0
125542061 12554206 5 C DIAZEPAM. DIAZEPAM 1 0
125542061 12554206 6 C RAMIPRIL. RAMIPRIL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125542061 12554206 1 Major depression

Outcome of event

Event ID CASEID OUTC COD
125542061 12554206 HO
125542061 12554206 DS
125542061 12554206 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125542061 12554206 Cardiomyopathy
125542061 12554206 Dyspnoea
125542061 12554206 Left ventricular dysfunction
125542061 12554206 Ventricular tachycardia

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
125542061 12554206 1 20000101 20160616 0