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
125137423 12513742 3 F 20140523 20160908 20160630 20160921 PER US-JNJFOC-20160523551 JANSSEN 68.51 YR E F Y 0.00000 20160921 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
125137423 12513742 1 SS XARELTO RIVAROXABAN 1 Oral U U UNKNOWN 0 10 MG TABLET
125137423 12513742 2 PS XARELTO RIVAROXABAN 1 Oral U U UNKNOWN 22406 10 MG TABLET
125137423 12513742 3 SS PLAVIX CLOPIDOGREL BISULFATE 1 Oral Y 0 75 MG UNSPECIFIED QD
125137423 12513742 4 SS ASPIRIN. ASPIRIN 1 Oral Y 0 81 MG UNSPECIFIED QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125137423 12513742 1 Deep vein thrombosis
125137423 12513742 2 Deep vein thrombosis
125137423 12513742 3 Product used for unknown indication
125137423 12513742 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125137423 12513742 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125137423 12513742 Lower 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
125137423 12513742 1 201406 0
125137423 12513742 2 20140425 20140502 0
125137423 12513742 3 20140501 0
125137423 12513742 4 20140501 0