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
123441232 12344123 2 F 20140119 20160614 20160507 20160912 PER US-JNJFOC-20160327509 JANSSEN 90.74 YR E F Y 0.00000 20160912 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
123441232 12344123 1 SS XARELTO RIVAROXABAN 1 Oral N UNKNOWN 0 15 MG TABLET
123441232 12344123 2 SS XARELTO RIVAROXABAN 1 Oral N UNKNOWN 0 15 MG TABLET
123441232 12344123 3 SS XARELTO RIVAROXABAN 1 Oral N UNKNOWN 0 15 MG TABLET
123441232 12344123 4 PS XARELTO RIVAROXABAN 1 Oral N UNKNOWN 202439 15 MG TABLET
123441232 12344123 5 SS NAPROXEN. NAPROXEN 1 Oral N UNKNOWN 0 500 MG TABLET BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123441232 12344123 1 Anticoagulant therapy
123441232 12344123 2 Atrial fibrillation
123441232 12344123 3 Thrombosis prophylaxis
123441232 12344123 4 Cerebrovascular accident prophylaxis
123441232 12344123 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123441232 12344123 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123441232 12344123 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
123441232 12344123 1 20130810 20140119 0
123441232 12344123 2 20130810 20140119 0
123441232 12344123 3 20130810 20140119 0
123441232 12344123 4 20130810 20140119 0
123441232 12344123 5 201401 0