The Safety Rates Drug Report

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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
125426411 12542641 1 I 20160624 20160709 20160709 EXP US-CIPLA LTD.-2016US08948 CIPLA TARHINI AA, ZAHOOR H, MCLAUGHLIN B, GOODING WE, SCHMITZ JC, SIEGFRIED JM ET AL.,. PHASE I TRIAL OF CARBOPLATIN AND ETOPOSIDE IN COMBINATION WITH PANOBINOSTAT IN PATIENTS WITH LUNG CANCER. ANTICANCER RESEARCH. 2013;33:4475 TO 4482 0.00 Y 0.00000 20160709 OT 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
125426411 12542641 1 PS CARBOPLATIN. CARBOPLATIN 1 Unknown AUC OF 5 ON DAY 1, EVERY 3 WEEKS U 77383
125426411 12542641 2 SS ETOPOSIDE. ETOPOSIDE 1 Unknown 100 MG/M2, ON DAYS 1, 2 AND 3, EVERY 3 WEEKS U 0 100 MG/M**2
125426411 12542641 3 SS Panobinostat PANOBINOSTAT 1 Oral 10 MG, THREE TIMES PER WEEK, GIVEN FOR 2 WEEKS, OUT OF A 3-WEEK CYCLE U 0 10 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125426411 12542641 1 Neuroendocrine carcinoma
125426411 12542641 2 Neuroendocrine carcinoma
125426411 12542641 3 Neuroendocrine carcinoma

Outcome of event

Event ID CASEID OUTC COD
125426411 12542641 DE
125426411 12542641 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125426411 12542641 Disease progression
125426411 12542641 Febrile neutropenia
125426411 12542641 Neutropenia
125426411 12542641 Thrombocytopenia

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

no results found

Therapies reported

no results found