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
127598931 12759893 1 I 20160426 20160603 20160919 20160919 EXP PHHO2016US008233 NOVARTIS 67.00 YR F Y 69.31000 KG 20160919 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
127598931 12759893 1 PS PAZOPANIB PAZOPANIB 1 Oral 3000 MG, UNK Y 22465 3000 MG
127598931 12759893 2 SS IFOSFAMIDE. IFOSFAMIDE 1 Intravenous (not otherwise specified) 1177 MG, UNK Y 0 1177 MG
127598931 12759893 3 SS DOXORUBICIN DOXORUBICIN 1 Intravenous (not otherwise specified) 132.76 MG, UNK Y 0 132.76 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127598931 12759893 1 Soft tissue neoplasm
127598931 12759893 2 Soft tissue neoplasm
127598931 12759893 3 Soft tissue neoplasm

Outcome of event

Event ID CASEID OUTC COD
127598931 12759893 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127598931 12759893 Fatigue
127598931 12759893 Pseudomonas infection
127598931 12759893 Sepsis
127598931 12759893 Soft tissue necrosis

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
127598931 12759893 1 20160412 20160509 0
127598931 12759893 2 20160503 20160504 0
127598931 12759893 3 20160503 20160504 0