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
118844624 11884462 4 F 20160204 20160104 20160210 PER US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2015-092968 BRISTOL MYERS SQUIBB 0.00 F Y 0.00000 20160210 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
118844624 11884462 1 PS ELIQUIS APIXABAN 1 Oral 5 MG, BID 5A879765 202155 5 MG BID
118844624 11884462 2 C CARVEDILOL. CARVEDILOL 1 Unknown 0
118844624 11884462 3 C LOSARTAN. LOSARTAN 1 Unknown 0
118844624 11884462 4 C TRAMADOL. TRAMADOL 1 Unknown 0
118844624 11884462 5 C MVI /01825701/ VITAMINS 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118844624 11884462 1 Cerebrovascular accident prophylaxis
118844624 11884462 2 Product used for unknown indication
118844624 11884462 3 Product used for unknown indication
118844624 11884462 4 Product used for unknown indication
118844624 11884462 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
118844624 11884462 Fatigue
118844624 11884462 Myalgia

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
118844624 11884462 1 20150721 0