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
127327501 12732750 1 I 201502 20160819 20160912 20160912 PER US-JNJFOC-20160820068 JANSSEN 68.09 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
127327501 12732750 1 SS XARELTO RIVAROXABAN 1 Oral U U 0 20 MG TABLET QD
127327501 12732750 2 SS XARELTO RIVAROXABAN 1 Oral U U 0 20 MG TABLET QD
127327501 12732750 3 SS XARELTO RIVAROXABAN 1 Oral U U 0 15 MG TABLET QD
127327501 12732750 4 SS XARELTO RIVAROXABAN 1 Oral U U 0 20 MG TABLET QD
127327501 12732750 5 SS XARELTO RIVAROXABAN 1 Oral U U 0 20 MG TABLET QD
127327501 12732750 6 SS XARELTO RIVAROXABAN 1 Oral U U 0 20 MG TABLET QD
127327501 12732750 7 SS XARELTO RIVAROXABAN 1 Oral U U 0 15 MG TABLET QD
127327501 12732750 8 SS XARELTO RIVAROXABAN 1 Oral U U 0 20 MG TABLET QD
127327501 12732750 9 SS XARELTO RIVAROXABAN 1 Oral U U 0 20 MG TABLET QD
127327501 12732750 10 SS XARELTO RIVAROXABAN 1 Oral U U 0 15 MG TABLET QD
127327501 12732750 11 SS XARELTO RIVAROXABAN 1 Oral U U 0 20 MG TABLET QD
127327501 12732750 12 PS XARELTO RIVAROXABAN 1 Oral U U 202439 20 MG TABLET QD
127327501 12732750 13 SS LOVENOX ENOXAPARIN SODIUM 1 Unknown Y 0 UNSPECIFIED
127327501 12732750 14 SS LOVENOX ENOXAPARIN SODIUM 1 Unknown Y 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127327501 12732750 1 Atrial fibrillation
127327501 12732750 2 Atrial fibrillation
127327501 12732750 3 Atrial fibrillation
127327501 12732750 4 Atrial fibrillation
127327501 12732750 5 Thrombosis prophylaxis
127327501 12732750 6 Thrombosis prophylaxis
127327501 12732750 7 Thrombosis prophylaxis
127327501 12732750 8 Thrombosis prophylaxis
127327501 12732750 9 Cerebrovascular accident prophylaxis
127327501 12732750 10 Cerebrovascular accident prophylaxis
127327501 12732750 11 Cerebrovascular accident prophylaxis
127327501 12732750 12 Cerebrovascular accident prophylaxis
127327501 12732750 13 Product used for unknown indication
127327501 12732750 14 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127327501 12732750 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127327501 12732750 Anaemia
127327501 12732750 Intra-abdominal haematoma
127327501 12732750 Shock haemorrhagic

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
127327501 12732750 1 20140320 20140415 0
127327501 12732750 2 20140416 0
127327501 12732750 3 20141219 20150105 0
127327501 12732750 4 2015 20150204 0
127327501 12732750 5 20140416 0
127327501 12732750 6 2015 20150204 0
127327501 12732750 7 20141219 20150105 0
127327501 12732750 8 20140320 20140415 0
127327501 12732750 9 2015 20150204 0
127327501 12732750 10 20141219 20150105 0
127327501 12732750 11 20140320 20140415 0
127327501 12732750 12 20140416 0
127327501 12732750 13 201502 0
127327501 12732750 14 20150207 20150213 0