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
120116612 12011661 2 F 20160826 20160205 20160826 EXP CH-BAYER-2016-019609 BAYER 55.00 YR A M Y 0.00000 20160826 CN GB CH

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
120116612 12011661 1 PS ACETYLSALICYLIC ACID (} 100 mg) ASPIRIN 1 100 MG, QD 21317 100 MG EFFERVESCENT TABLET QD
120116612 12011661 2 SS ACETYLSALICYLIC ACID (} 100 mg) ASPIRIN 1 21317 EFFERVESCENT TABLET
120116612 12011661 3 SS CLOPIDOGREL CLOPIDOGREL BISULFATE 1 75 MG, QD 0 75 MG QD
120116612 12011661 4 SS CLOPIDOGREL CLOPIDOGREL BISULFATE 1 75 MG, QD 0 75 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
120116612 12011661 1 Platelet aggregation inhibition
120116612 12011661 2 Arthralgia
120116612 12011661 3 Platelet aggregation inhibition
120116612 12011661 4 Arthralgia

Outcome of event

Event ID CASEID OUTC COD
120116612 12011661 LT
120116612 12011661 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
120116612 12011661 Drug interaction
120116612 12011661 Haemoptysis
120116612 12011661 Product use issue

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found