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
102787032 10278703 2 F 20160713 20140704 20160715 EXP TR-BRISTOL-MYERS SQUIBB COMPANY-21159595 BRISTOL MYERS SQUIBB 49.00 YR M Y 0.00000 20160715 CN TR TR

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
102787032 10278703 1 PS WARFARIN SODIUM. WARFARIN SODIUM 1 Unknown TABS U 9218 .5 MG
102787032 10278703 2 C VERAPAMIL VERAPAMIL HYDROCHLORIDE 1 Unknown TABS U 0 120 MG
102787032 10278703 3 C ALBUTEROL. ALBUTEROL 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
102787032 10278703 1 Product used for unknown indication
102787032 10278703 2 Product used for unknown indication
102787032 10278703 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
102787032 10278703 LT
102787032 10278703 OT
102787032 10278703 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
102787032 10278703 Activated partial thromboplastin time
102787032 10278703 Dyspnoea
102787032 10278703 Haemoptysis
102787032 10278703 International normalised ratio increased
102787032 10278703 Prothrombin time prolonged
102787032 10278703 Pulmonary alveolar haemorrhage
102787032 10278703 Respiratory failure
102787032 10278703 Tachypnoea

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found