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
126705604 12670560 4 F 20160512 20160928 20160822 20160928 EXP GB-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-066473 BRISTOL MYERS SQUIBB 50.91 YR M Y 0.00000 20160928 CN GB GB

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
126705604 12670560 1 PS APIXABAN APIXABAN 1 Unknown UNK U U 202155
126705604 12670560 2 SS AMIODARONE AMIODARONE 1 Unknown UNK U U 0 SOLUTION FOR INJECTION
126705604 12670560 3 SS BISOPROLOL BISOPROLOL 1 Unknown UNK U U 0
126705604 12670560 4 SS DIAZEPAM. DIAZEPAM 1 Oral UNK U U 0
126705604 12670560 5 SS HEPARIN HEPARIN SODIUM 1 Intravenous (not otherwise specified) UNK Y U 0
126705604 12670560 6 SS MONOPARIN HEPARIN SODIUM 1 Subcutaneous 0.2ML Y U 0 .2 ML
126705604 12670560 7 SS ELIQUIS APIXABAN 1 U U 0
126705604 12670560 8 SS HEPARIN HEPARIN SODIUM 1 Intravenous (not otherwise specified) Y U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126705604 12670560 1 Product used for unknown indication
126705604 12670560 2 Product used for unknown indication
126705604 12670560 3 Product used for unknown indication
126705604 12670560 4 Product used for unknown indication
126705604 12670560 5 Product used for unknown indication
126705604 12670560 6 Product used for unknown indication
126705604 12670560 8 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126705604 12670560 HO
126705604 12670560 LT
126705604 12670560 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126705604 12670560 Asthenia
126705604 12670560 Asthma
126705604 12670560 Atrial fibrillation
126705604 12670560 Back pain
126705604 12670560 Cardiac failure
126705604 12670560 Complication associated with device
126705604 12670560 Contraindicated product administered
126705604 12670560 Dialysis
126705604 12670560 Discomfort
126705604 12670560 General physical condition abnormal
126705604 12670560 Heart rate abnormal
126705604 12670560 Hepatic failure
126705604 12670560 Insomnia
126705604 12670560 Internal haemorrhage
126705604 12670560 Jaundice
126705604 12670560 Limb discomfort
126705604 12670560 Malaise
126705604 12670560 Monoplegia
126705604 12670560 Muscle haemorrhage
126705604 12670560 Poor peripheral circulation
126705604 12670560 Productive cough
126705604 12670560 Pyrexia
126705604 12670560 Renal failure
126705604 12670560 Sensory disturbance
126705604 12670560 Septic rash
126705604 12670560 Septic shock
126705604 12670560 Tachycardia
126705604 12670560 Thrombocytopenia

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
126705604 12670560 4 20160512 0
126705604 12670560 5 20160512 2016 0
126705604 12670560 6 20160512 20160615 0
126705604 12670560 8 20160512 0