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
127035451 12703545 1 I 20151019 20160519 20160831 20160831 EXP US-BAYER-2016-102138 BAYER 87.00 YR E F Y 0.00000 20160831 OT 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
127035451 12703545 1 SS XARELTO RIVAROXABAN 1 Oral UNK N UNKNOWN 0 FILM-COATED TABLET
127035451 12703545 2 SS XARELTO RIVAROXABAN 1 Oral UNK N UNKNOWN 0 FILM-COATED TABLET
127035451 12703545 3 SS XARELTO RIVAROXABAN 1 N 0 FILM-COATED TABLET
127035451 12703545 4 PS ACETYLSALICYLIC ACID({=100 mg) ASPIRIN 1 Oral 81 MG, UNK 999999 81 MG TABLET
127035451 12703545 5 SS NAPROXEN. NAPROXEN 1 Oral 500 MG, UNK 0 500 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127035451 12703545 1 Thrombosis prophylaxis
127035451 12703545 2 Cerebrovascular accident prophylaxis
127035451 12703545 3 Atrial fibrillation
127035451 12703545 4 Product used for unknown indication
127035451 12703545 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127035451 12703545 HO
127035451 12703545 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
127035451 12703545 Acute kidney injury
127035451 12703545 Cerebrovascular accident
127035451 12703545 Petechiae

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
127035451 12703545 1 201507 0
127035451 12703545 2 201510 20151018 0
127035451 12703545 4 201510 0
127035451 12703545 5 201510 0