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
76306564 7630656 4 F 20081113 20121221 20101015 20121231 EXP CN-MPIJNJ-2010-05188 MILLENNIUM 0.00 Y 0.00000 20121231 CN CN CN

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
76306564 7630656 1 PS VELCADE 1 INTRAVENOUS 2.4 MG, UNK D NOT REPORTED 21602 2.4 MG Injection
76306564 7630656 2 SS VELCADE 1 INTRAVENOUS 2.2 MG, UNK D NOT REPORTED 21602 2.2 MG Injection
76306564 7630656 3 C ADRIAMYCIN /00330901/ 1 U 0
76306564 7630656 4 C DEXAMETHASONE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
76306564 7630656 1 MULTIPLE MYELOMA

Outcome of event

Event ID CASEID OUTC COD
76306564 7630656 OT
76306564 7630656 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
76306564 7630656 Bone marrow failure
76306564 7630656 Circulatory collapse
76306564 7630656 Dehydration
76306564 7630656 Diarrhoea
76306564 7630656 Electrolyte imbalance
76306564 7630656 Gastroenteritis
76306564 7630656 Haematuria
76306564 7630656 Hypokalaemia
76306564 7630656 Hypotension
76306564 7630656 Lung infection
76306564 7630656 Nausea
76306564 7630656 Plasma cell myeloma
76306564 7630656 Pneumonia
76306564 7630656 Pyrexia
76306564 7630656 Respiratory failure
76306564 7630656 Thrombocytopenia
76306564 7630656 Urinary retention
76306564 7630656 Vomiting

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
76306564 7630656 2 20081114 0