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
82992732 8299273 2 F 20110817 20160823 20111219 20160929 EXP US-ROCHE-1022834 ROCHE 69.00 YR F Y 52.00000 KG 20160929 MD 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
82992732 8299273 1 PS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) 10MG/ KG IV OVER 30-90 MIN ON DAYS 1 AND 15 Y 125085 SOLUTION FOR INFUSION
82992732 8299273 2 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) 25MG ON DAYS 1,8, 15, 22, TEMPORARILY INTERRUPTED Y 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
82992732 8299273 1 Hepatocellular carcinoma
82992732 8299273 2 Hepatocellular carcinoma

Outcome of event

Event ID CASEID OUTC COD
82992732 8299273 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
82992732 8299273 Abdominal pain
82992732 8299273 Chills
82992732 8299273 Nausea
82992732 8299273 Pyrexia
82992732 8299273 Vomiting

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
82992732 8299273 1 20110812 20110906 0
82992732 8299273 2 20110812 20110906 0