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
126518801 12651880 1 I 20150505 20160517 20160815 20160815 EXP US-BAYER-2016-101869 BAYER 75.00 YR E M Y 0.00000 20160815 OT 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
126518801 12651880 1 SS XARELTO RIVAROXABAN 1 Oral 20 MG, UNK Y UNKNOWN 0 FILM-COATED TABLET
126518801 12651880 2 SS PLAVIX CLOPIDOGREL BISULFATE 1 Oral 75 MG, QD Y 0 75 MG QD
126518801 12651880 3 SS PLAVIX CLOPIDOGREL BISULFATE 1 Y 0
126518801 12651880 4 PS ACETYLSALICYLIC ACID({=100 mg) ASPIRIN 1 Oral 81 MG, QD Y 999999 81 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126518801 12651880 1 Product used for unknown indication
126518801 12651880 2 Product used for unknown indication
126518801 12651880 3 Product used for unknown indication
126518801 12651880 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126518801 12651880 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126518801 12651880 Gastrointestinal haemorrhage
126518801 12651880 Haemoptysis

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
126518801 12651880 1 20140922 20150720 0
126518801 12651880 2 20150720 0
126518801 12651880 4 20150720 0