The Safety Rates Drug Report

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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
123444013 12344401 3 F 201405 20160628 20160507 20160725 PER US-JNJFOC-20160402267 JANSSEN 66.23 YR E F Y 0.00000 20160725 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
123444013 12344401 1 SS XARELTO RIVAROXABAN 1 Oral VARYING DOSES OF 15 MG, 20 MG Y N UNKNOWN 0 TABLET
123444013 12344401 2 SS XARELTO RIVAROXABAN 1 Oral VARYING DOSES OF 15 MG, 20 MG Y N UNKNOWN 0 TABLET
123444013 12344401 3 SS XARELTO RIVAROXABAN 1 Oral VARYING DOSES OF 15 MG, 20 MG Y N UNKNOWN 0 TABLET
123444013 12344401 4 PS XARELTO RIVAROXABAN 1 Oral VARYING DOSES OF 15 MG, 20 MG Y N UNKNOWN 22406 TABLET
123444013 12344401 5 SS MOTRIN IBUPROFEN 1 Oral Y N UNKNOWN 17463 800 MG TABLETS

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123444013 12344401 1 Thrombosis prophylaxis
123444013 12344401 2 Thrombosis prophylaxis
123444013 12344401 3 Thrombosis prophylaxis
123444013 12344401 4 Thrombosis prophylaxis
123444013 12344401 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123444013 12344401 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123444013 12344401 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
123444013 12344401 1 201510 0
123444013 12344401 2 20131223 20140612 0
123444013 12344401 3 201510 0
123444013 12344401 4 20131223 20140612 0