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
127827011 12782701 1 I 20160906 20160919 20160927 20160927 EXP GB-MHRA-ADR 23644926 GB-ACCORD-044316 ACCORD 72.00 YR F Y 0.00000 20160927 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
127827011 12782701 1 PS AMOXICILLIN. AMOXICILLIN 1 Oral Y 200750232 500 MG
127827011 12782701 2 SS RAMIPRIL. RAMIPRIL 1 Oral Y 202392 1.25 MG
127827011 12782701 3 C ACETYLSALICYLIC ACID ASPIRIN 1 0
127827011 12782701 4 C ATENOLOL/ATENOLOL HYDROCHLORIDE 2 0
127827011 12782701 5 C BENDROFLUMETHIAZIDE BENDROFLUMETHIAZIDE 1 0
127827011 12782701 6 C SIMVASTATIN. SIMVASTATIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127827011 12782701 1 Product used for unknown indication
127827011 12782701 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127827011 12782701 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127827011 12782701 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
127827011 12782701 1 20160904 0
127827011 12782701 2 20160817 0