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
125519981 12551998 1 I 201508 20160629 20160713 20160713 EXP PHHY2016DE091143 NOVARTIS 42.00 YR M Y 0.00000 20160713 DE DE

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
125519981 12551998 1 PS PANOBINOSTAT PANOBINOSTAT 1 Unknown U 205353
125519981 12551998 2 SS VINCRISTINE SULFATE. VINCRISTINE SULFATE 1 Unknown U 0
125519981 12551998 3 SS DEXAMETHASONE. DEXAMETHASONE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125519981 12551998 1 Acute lymphocytic leukaemia
125519981 12551998 2 Acute lymphocytic leukaemia
125519981 12551998 3 Acute lymphocytic leukaemia

Outcome of event

Event ID CASEID OUTC COD
125519981 12551998 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125519981 12551998 Acute lymphocytic leukaemia
125519981 12551998 Facial paresis
125519981 12551998 Malignant neoplasm progression
125519981 12551998 Off label use

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

no results found

Therapies reported

no results found