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
125204051 12520405 1 I 20160617 20160701 20160701 EXP US-BAUSCH-BL-2016-015252 BAUSCH AND LOMB 93.00 YR F Y 56.75000 KG 20160701 CN US US

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
125204051 12520405 1 PS NIFEDICAL XL NIFEDIPINE 1 Unknown 75289 EXTENDED-RELEASE TABLET
125204051 12520405 2 SS CLOPIDOGREL CLOPIDOGREL BISULFATE 1 Unknown 0 TABLET QOD
125204051 12520405 3 SS LOSARTAN POTASSIUM. LOSARTAN POTASSIUM 1 Unknown U 0 TABLET
125204051 12520405 4 SS LOSARTAN POTASSIUM. LOSARTAN POTASSIUM 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125204051 12520405 1 Hypertension
125204051 12520405 2 Prophylaxis
125204051 12520405 3 Transient ischaemic attack
125204051 12520405 4 Hypertension

Outcome of event

Event ID CASEID OUTC COD
125204051 12520405 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125204051 12520405 Balance disorder
125204051 12520405 Dizziness
125204051 12520405 Rectal haemorrhage

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
125204051 12520405 2 2014 0
125204051 12520405 3 2014 20151016 0