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
127378341 12737834 1 I 20160813 0 20160909 20160909 DIR FDA-CTU 70.78 YR F N 60.30000 KG 20160908 N MD 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
127378341 12737834 1 PS DEXAMETHASONE. DEXAMETHASONE 1 0 120 MG
127378341 12737834 2 SS LENALIDOMIDE (CC-5013) LENALIDOMIDE 1 0 250 MG
127378341 12737834 3 SS VELCADE BORTEZOMIB 1 0 4 MG
127378341 12737834 5 C OXYCONTIN OXYCODONE HYDROCHLORIDE 1 0
127378341 12737834 7 C GABAPENTIN. GABAPENTIN 1 0
127378341 12737834 9 C OXYCODONE OXYCODONE 1 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
127378341 12737834 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127378341 12737834 Back pain
127378341 12737834 Confusional state
127378341 12737834 Haemoglobin decreased
127378341 12737834 Hyperglycaemia
127378341 12737834 Hyponatraemia
127378341 12737834 Lethargy
127378341 12737834 Mental status changes
127378341 12737834 Metabolic acidosis
127378341 12737834 Neutropenia
127378341 12737834 Oxygen saturation decreased
127378341 12737834 Pancytopenia
127378341 12737834 Pneumonia
127378341 12737834 Pyrexia
127378341 12737834 Sepsis
127378341 12737834 Somnolence
127378341 12737834 Urinary tract infection

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
127378341 12737834 1 20160816 0
127378341 12737834 2 20160816 0
127378341 12737834 3 20160816 0