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
125615651 12561565 1 I 20160706 20160715 20160715 EXP PHHY2016GB093396 SANDOZ 0.00 F Y 0.00000 20160715 OT GB GB

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
125615651 12561565 1 PS PACLITAXEL. PACLITAXEL 1 Unknown U 78167
125615651 12561565 2 SS AVASTIN BEVACIZUMAB 1 Unknown U UNAVAILABLE 0
125615651 12561565 3 C XGEVA DENOSUMAB 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125615651 12561565 1 Product used for unknown indication
125615651 12561565 2 Product used for unknown indication
125615651 12561565 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125615651 12561565 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125615651 12561565 Alopecia
125615651 12561565 Arthralgia
125615651 12561565 Epistaxis
125615651 12561565 Fatigue
125615651 12561565 Hepatic pain
125615651 12561565 Metastases to central nervous system
125615651 12561565 Oropharyngeal pain
125615651 12561565 Productive cough
125615651 12561565 Viral upper respiratory tract infection

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

no results found

Therapies reported

no results found