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
112686404 11268640 4 F 20140813 20160720 20150714 20160801 EXP US-JNJFOC-20150704859 JANSSEN 62.93 YR A F Y 90.27000 KG 20160801 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
112686404 11268640 1 SS XARELTO RIVAROXABAN 1 Oral U U UNKNOWN 0 TABLET
112686404 11268640 2 PS XARELTO RIVAROXABAN 1 Oral U U UNKNOWN 22406 10 MG TABLET
112686404 11268640 3 SS AGGRENOX ASPIRINDIPYRIDAMOLE 1 U 0
112686404 11268640 4 C LISINOPRIL. LISINOPRIL 1 0
112686404 11268640 5 C HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 0
112686404 11268640 6 C PRILOSEC OMEPRAZOLE MAGNESIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
112686404 11268640 1 Deep vein thrombosis
112686404 11268640 2 Deep vein thrombosis
112686404 11268640 3 Product used for unknown indication
112686404 11268640 4 Product used for unknown indication
112686404 11268640 5 Product used for unknown indication
112686404 11268640 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
112686404 11268640 HO
112686404 11268640 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
112686404 11268640 Anaemia
112686404 11268640 Lower gastrointestinal haemorrhage
112686404 11268640 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
112686404 11268640 1 20140801 20141016 0
112686404 11268640 2 20140715 20141002 0