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
119720314 11972031 4 F 20151103 20160818 20160128 20160824 EXP PHJP2016JP001063 NOVARTIS 57.94 YR M Y 65.00000 KG 20160824 JP JP

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
119720314 11972031 1 PS FARYDAK PANOBINOSTAT 1 Oral 20 MG, QD 240 MG Y U 205353 20 MG CAPSULE QD
119720314 11972031 2 SS BORTEZOMIB BORTEZOMIB 1 Unknown 1.3 MG/M2, UNK Y 0 1.3 MG/M**2
119720314 11972031 3 SS DEXAMETHASONE. DEXAMETHASONE 1 Unknown 20 MG, UNK Y 0 20 MG
119720314 11972031 4 C LOPERAMIDE LOPERAMIDE 1 Unknown Y 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119720314 11972031 1 Plasma cell myeloma
119720314 11972031 2 Plasma cell myeloma
119720314 11972031 3 Plasma cell myeloma
119720314 11972031 4 Prophylaxis

Outcome of event

Event ID CASEID OUTC COD
119720314 11972031 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
119720314 11972031 Abdominal pain
119720314 11972031 Constipation
119720314 11972031 Faeces soft
119720314 11972031 Ileus
119720314 11972031 Malignant neoplasm progression
119720314 11972031 Nausea
119720314 11972031 Plasma cell myeloma
119720314 11972031 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
119720314 11972031 1 20151027 20151221 0