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
125691972 12569197 2 F 20160707 20160816 20160719 20160824 EXP US-CELGENEUS-USA-2016072504 CELGENE 78.00 YR F Y 59.00000 KG 20160824 OT 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
125691972 12569197 1 PS ABRAXANE PACLITAXEL 1 Intravenous drip 100 MILLIGRAM/SQ. METER Y U 21660 100 MG/M**2 INJECTION FOR INFUSION
125691972 12569197 2 SS FUROSEMIDE. FUROSEMIDE 1 Oral U U 0 40 MG UNKNOWN BID
125691972 12569197 3 SS SPIRONOLACTONE. SPIRONOLACTONE 1 Oral U U 0 25 MG UNKNOWN QD
125691972 12569197 4 C LASIX FUROSEMIDE 1 Unknown 0 UNKNOWN
125691972 12569197 5 C ALDACTONE SPIRONOLACTONE 1 Unknown 0 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125691972 12569197 1 Non-small cell lung cancer
125691972 12569197 2 Oedema peripheral
125691972 12569197 3 Oedema peripheral
125691972 12569197 4 Product used for unknown indication
125691972 12569197 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125691972 12569197 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125691972 12569197 Acute kidney injury
125691972 12569197 Asthenia
125691972 12569197 Fall
125691972 12569197 Haemoptysis

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
125691972 12569197 1 20160610 0
125691972 12569197 2 201508 20160707 0
125691972 12569197 3 201508 20160707 0
125691972 12569197 4 201508 201607 0
125691972 12569197 5 201508 201607 0