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
125607411 12560741 1 I 20160509 20160701 20160715 20160715 EXP DE-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-120266 RANBAXY 64.00 YR M Y 80.00000 KG 20160715 OT DE DE

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
125607411 12560741 1 PS CLARITHROMYCIN. CLARITHROMYCIN 1 Oral 250 MG, BID 2500 MG U U 65174 250 MG Q12H
125607411 12560741 2 C RAMIPRIL. RAMIPRIL 1 Oral 2.5 MG, QD U U 0 2.5 MG
125607411 12560741 3 C Bisoprolol BISOPROLOL 1 Oral 2.5 MG, QD U U 0 2.5 MG
125607411 12560741 4 C Atorvastatin ATORVASTATIN 1 Oral 10 MG, QD U U 0 10 MG
125607411 12560741 5 C Ass 100 ASPIRIN 1 Oral 100 MG, QD U U 0 100 MG
125607411 12560741 6 C Paracetamol ACETAMINOPHEN 1 Oral 1 DF, BID U U 0 1 DF Q12H

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125607411 12560741 1 Upper respiratory tract infection
125607411 12560741 2 Coronary artery disease
125607411 12560741 3 Coronary artery disease
125607411 12560741 4 Hyperlipidaemia
125607411 12560741 5 Coronary artery disease
125607411 12560741 6 Infection

Outcome of event

Event ID CASEID OUTC COD
125607411 12560741 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125607411 12560741 Liver function test abnormal
125607411 12560741 Malaise
125607411 12560741 Somnolence

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
125607411 12560741 1 20160502 20160506 0
125607411 12560741 6 20160502 20160502 0