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
90687551 9068755 1 I 20121209 0 20130212 20130212 DIR 54.53 YR M N 87.60000 KG 20130201 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
90687551 9068755 1 PS BIBF 1120 1 D D E07655-001L02-105417,E07655-001L02-105418,E07655-001L02-105419 20131130 0 200 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
90687551 9068755 1 Glioblastoma multiforme

Outcome of event

Event ID CASEID OUTC COD
90687551 9068755 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
90687551 9068755 Abasia
90687551 9068755 Asthenia
90687551 9068755 Disseminated intravascular coagulation
90687551 9068755 Haematoma
90687551 9068755 Haemorrhage intracranial
90687551 9068755 Hypokalaemia
90687551 9068755 Pneumonia
90687551 9068755 Thrombocytopenia
90687551 9068755 Thrombosis in device

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
90687551 9068755 1 20121016 20121113 0