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
127916611 12791661 1 I 20160906 20160919 20160929 20160929 EXP GB-MHRA-EYC 00145258 GB-TEVA-694963ACC TEVA 72.00 YR F Y 0.00000 20160929 PH 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
127916611 12791661 1 PS RAMIPRIL. RAMIPRIL 1 Oral Y U 77470 1.25 MG
127916611 12791661 2 SS AMOXICILLIN. AMOXICILLIN 1 Oral Y U 0 500 MG
127916611 12791661 3 C ASPIRIN. ASPIRIN 1 0
127916611 12791661 4 C ATENOLOL. ATENOLOL 1 0
127916611 12791661 5 C BENDROFLUMETHIAZIDE BENDROFLUMETHIAZIDE 1 0
127916611 12791661 6 C SIMVASTATIN. SIMVASTATIN 1 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
127916611 12791661 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127916611 12791661 Anaphylactic reaction

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
127916611 12791661 1 20160817 0
127916611 12791661 2 20160904 0