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
125075443 12507544 3 F 20160612 20160804 20160629 20160808 EXP JP-ELI_LILLY_AND_COMPANY-JP201606008114 ELI LILLY AND CO 73.00 YR M Y 50.30000 KG 20160808 CN JP JP

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
125075443 12507544 1 PS CYRAMZA RAMUCIRUMAB 1 Intravenous (not otherwise specified) 420 MG, 2/W 10080 MG Y 125477 420 MG INJECTION BIW
125075443 12507544 2 SS PACLITAXEL. PACLITAXEL 1 Intravenous (not otherwise specified) 130 MG, DAY 1, 8 AND 15 OF 28-DAY CYCLE Y 0 130 MG
125075443 12507544 3 C HIRUDOID /00723701/ PENTOSAN POLYSULFATE SODIUM 1 Transdermal UNK 0 OINTMENT
125075443 12507544 4 C KENALOG TRIAMCINOLONE ACETONIDE 1 Transdermal UNK 0 OINTMENT

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125075443 12507544 1 Gastric cancer recurrent
125075443 12507544 2 Gastric cancer recurrent
125075443 12507544 3 Dry skin
125075443 12507544 4 Stomatitis

Outcome of event

Event ID CASEID OUTC COD
125075443 12507544 HO
125075443 12507544 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125075443 12507544 Beta haemolytic streptococcal infection
125075443 12507544 Disseminated intravascular coagulation
125075443 12507544 Febrile neutropenia
125075443 12507544 Septic shock

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
125075443 12507544 1 20160317 20160609 0
125075443 12507544 2 20160317 20160609 0
125075443 12507544 3 20160324 20160609 0
125075443 12507544 4 20160609 20160609 0