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
116959338 11695933 8 F 20150626 20160916 20151104 20160926 EXP PHHO2015FR017366 NOVARTIS 69.17 YR M Y 77.00000 KG 20160926 MD FR FR

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
116959338 11695933 1 PS PAZOPANIB PAZOPANIB 1 Oral 400 MG, UNK 22465 400 MG TABLET
116959338 11695933 2 SS GEMCITABINE GEMCITABINEGEMCITABINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) 1250 MG, UNK 0 1250 MG
116959338 11695933 3 C METFORMIN W/SITAGLIPTIN METFORMINSITAGLIPTIN PHOSPHATE 1 Oral U 0
116959338 11695933 4 C CRESTOR ROSUVASTATIN CALCIUM 1 Oral U 0
116959338 11695933 5 C BISOPROLOL BISOPROLOL 1 Oral U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
116959338 11695933 1 Soft tissue sarcoma
116959338 11695933 2 Soft tissue sarcoma
116959338 11695933 3 Diabetes mellitus
116959338 11695933 4 Hyperlipidaemia
116959338 11695933 5 Hypertension

Outcome of event

Event ID CASEID OUTC COD
116959338 11695933 HO
116959338 11695933 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
116959338 11695933 Febrile bone marrow aplasia
116959338 11695933 Neutropenia

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
116959338 11695933 1 20150610 20151014 0
116959338 11695933 2 20150610 20151008 0