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
119836002 11983600 2 F 201304 20160805 20160201 20160816 EXP US-BAYER-2014-054074 BAYER 72.00 YR E F Y 0.00000 20160816 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
119836002 11983600 1 SS XARELTO RIVAROXABAN 1 Oral UNK N UNKNOWN 0 20 MG FILM-COATED TABLET
119836002 11983600 2 SS XARELTO RIVAROXABAN 1 N 0 FILM-COATED TABLET
119836002 11983600 3 SS TYLENOL ACETAMINOPHEN 1 Unknown 650 MG, QID 0 650 MG QID
119836002 11983600 4 PS ACETYLSALICYLIC ACID({=100 mg) ASPIRIN 1 Unknown 81 MG, UNK 999999 81 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119836002 11983600 1 Atrial fibrillation
119836002 11983600 2 Cerebrovascular accident prophylaxis
119836002 11983600 3 Product used for unknown indication
119836002 11983600 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
119836002 11983600 HO
119836002 11983600 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
119836002 11983600 Gastrointestinal 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
119836002 11983600 1 201301 201304 0