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
127107671 12710767 1 I 201601 20160823 20160902 20160902 EXP US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-070006 BRISTOL MYERS SQUIBB 43.20 YR F Y 104.30000 KG 20160902 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
127107671 12710767 1 PS COUMADIN WARFARIN SODIUM 1 Unknown U 9218
127107671 12710767 2 SS ADCIRCA TADALAFIL 1 Unknown U 0
127107671 12710767 3 SS LETAIRIS AMBRISENTAN 1 Oral 10 MG, QD U 1500226A 0 10 MG TABLET QD
127107671 12710767 4 SS ORENITRAM TREPROSTINIL 1 Oral 13.5 MG, TID U 2100399 0 13.5 MG TID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127107671 12710767 1 Product used for unknown indication
127107671 12710767 2 Product used for unknown indication
127107671 12710767 3 Product used for unknown indication
127107671 12710767 4 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
127107671 12710767 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127107671 12710767 Cough
127107671 12710767 Diarrhoea
127107671 12710767 Dizziness
127107671 12710767 Flushing
127107671 12710767 Malaise
127107671 12710767 Oedema peripheral
127107671 12710767 Oropharyngeal pain
127107671 12710767 Pain in extremity
127107671 12710767 Pneumonia
127107671 12710767 Sinus disorder

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
127107671 12710767 3 20130823 0
127107671 12710767 4 20150819 0