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
127448901 12744890 1 I 20100214 20110113 20160915 20160915 EXP US-ROCHE-756242 ROCHE 76.00 YR F Y 73.00000 KG 20160915 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
127448901 12744890 1 PS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) OVER 30 TO 90 MIN ON DAYS 1 AND 15, CYCLE 28 DAYS (CYCLE 1) 125085 1500 MG SOLUTION FOR INFUSION
127448901 12744890 2 SS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) OVER 30 TO 90 MIN ON DAYS 1 AND 15, CYCLE 28 DAYS (CYCLE 2) 125085 1460 MG SOLUTION FOR INFUSION
127448901 12744890 3 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) ON DAYS 1,8, 15, 22, CYCLE 28 DAYS 0 100 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127448901 12744890 1 Ovarian neoplasm
127448901 12744890 3 Ovarian neoplasm

Outcome of event

Event ID CASEID OUTC COD
127448901 12744890 DE
127448901 12744890 HO
127448901 12744890 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127448901 12744890 Ascites
127448901 12744890 Blood fibrinogen decreased
127448901 12744890 Death
127448901 12744890 Dehydration
127448901 12744890 Fatigue
127448901 12744890 Malignant pleural effusion
127448901 12744890 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
127448901 12744890 2 20100118 20100209 0
127448901 12744890 3 20091207 20100209 0