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
6138536 6920599 F 6138536-8 20090211 20090325 20090331 EXP NL-CELGENEUS-114-21880-09020877 CELGENEUS 77 M Y 88.1 KG 20090331 NETHERLANDS

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
6138536 1011358244 PS REVLIMID 1 ORAL 021880
6138536 1011358245 SS REVLIMID 1 ORAL 021880
6138536 1011358246 C DEXAMETHASONE 2 ORAL
6138536 1011358247 C TOLBUTAMIDE 1 ORAL
6138536 1011358248 C SERETIDE 2 RESPIRATORY (INHALATION)
6138536 1011358249 C ACENOCOUMAROL 2 ORAL
6138536 1011358250 C COTRIMOXAZOLE 2 ORAL

Indications of drugs used

Event ID DRUG SEQ INDI PT
6138536 1011358244 MULTIPLE MYELOMA
6138536 1011358246 DRUG USE FOR UNKNOWN INDICATION
6138536 1011358247 DIABETES MELLITUS
6138536 1011358248 CHRONIC OBSTRUCTIVE PULMONARY DISEASE
6138536 1011358249 PROPHYLAXIS
6138536 1011358250 PROPHYLAXIS

Outcome of event

Event ID OUTC COD
6138536 HO
6138536 LT
6138536 OT

Reactions reported

Event ID PT
6138536 STOMATITIS
6138536 UROSEPSIS

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6138536 1011358244 20090112
6138536 1011358245 20090209 20090211
6138536 1011358246 20090112
6138536 1011358247 20020101
6138536 1011358248 20070101
6138536 1011358249 20080901
6138536 1011358250 20090107