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
126005091 12600509 1 I 201509 20160721 20160727 20160727 EXP FR-SA-2016SA134663 AVENTIS 80.00 YR E M Y 0.00000 20160727 OT FR FR

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
126005091 12600509 1 SS FUROSEMIDE. FUROSEMIDE 1 Unknown Y UNK 0 20 MG TABLET
126005091 12600509 2 PS IRBESARTAN. IRBESARTAN 1 Oral Y UNK 20757 150 MG TABLET QD
126005091 12600509 3 SS GABAPENTIN. GABAPENTIN 1 Oral Y UNK 0 200 MG TABLET TID
126005091 12600509 4 C PREVISCAN FLUINDIONE 1 Oral 0 15 MG QD
126005091 12600509 5 C ALLOPURINOL. ALLOPURINOL 1 Oral 0 100 MG TABLET QD
126005091 12600509 6 C CARAFATE SUCRALFATE 1 Oral 0
126005091 12600509 7 C CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Oral 0 10 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126005091 12600509 2 Hypertension
126005091 12600509 4 Atrial fibrillation
126005091 12600509 5 Hyperuricaemia
126005091 12600509 6 Peptic ulcer
126005091 12600509 7 Depression

Outcome of event

Event ID CASEID OUTC COD
126005091 12600509 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126005091 12600509 Fall

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
126005091 12600509 2 201509 20151001 0
126005091 12600509 6 201510 0