The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
5421858 6390508 I 5421858-3 20070807 20070820 EXP 2007SP016175 SCHERING-PLOUGH CORPORATION 63 YR M N 20070815 MD ISRAEL

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
5421858 1008833726 PS INTERFERON ALFA-2B RECOMBINANT (S-P) (INTERFERON ALFA-2B) 2 INTRAVENOUS 18 MIU; QD; IV D D
5421858 1008843376 C CYCLOPHOSPHAMIDE 1
5421858 1008843377 C ADRIAMYCIN PFS 1
5421858 1008843378 C VINCRISTINE 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
5421858 1008833726 MALIGNANT MELANOMA

Outcome of event

Event ID OUTC COD
5421858 HO

Reactions reported

Event ID PT
5421858 CARDIAC FAILURE CONGESTIVE
5421858 CARDIOMYOPATHY
5421858 CARDIOTOXICITY
5421858 HEPATIC ENZYME INCREASED
5421858 HYPOTENSION
5421858 LEFT VENTRICULAR DYSFUNCTION
5421858 MITRAL VALVE INCOMPETENCE
5421858 PLEURAL EFFUSION
5421858 PLEUROPERICARDITIS
5421858 TACHYPNOEA
5421858 WHITE BLOOD CELL COUNT INCREASED

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

Event ID RPSR COD
5421858 FGN
5421858 HP
5421858 LIT

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
5421858 1008833726 1 MON