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
119908014 11990801 4 F 20160111 20160811 20160202 20160823 EXP US-CELGENEUS-USA-2016016533 CELGENE 69.45 YR F Y 114.41000 KG 20160823 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
119908014 11990801 1 PS REVLIMID LENALIDOMIDE 1 Oral Y U UNKNOWN 21880 25 MG CAPSULES
119908014 11990801 2 SS REVLIMID LENALIDOMIDE 1 Oral Y U UNKNOWN 21880 15 MG CAPSULES
119908014 11990801 3 SS LOVENOX ENOXAPARIN SODIUM 1 Unknown U U 0 120 MG UNKNOWN QD
119908014 11990801 4 SS LOVENOX ENOXAPARIN SODIUM 1 U U 0
119908014 11990801 5 SS VELCADE BORTEZOMIB 1 Unknown U U 0 UNKNOWN
119908014 11990801 6 C ASPIRIN. ASPIRIN 1 Unknown 0 325 MG UNKNOWN QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119908014 11990801 1 Plasma cell myeloma
119908014 11990801 3 Pulmonary thrombosis
119908014 11990801 4 Haematuria
119908014 11990801 5 Product used for unknown indication
119908014 11990801 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
119908014 11990801 HO
119908014 11990801 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
119908014 11990801 Diarrhoea
119908014 11990801 Haematuria
119908014 11990801 Hypotension
119908014 11990801 Pulmonary thrombosis

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
119908014 11990801 1 20151120 20160209 0
119908014 11990801 2 20160217 20160316 0
119908014 11990801 3 20160111 20160712 0
119908014 11990801 6 20151104 0