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
123766131 12376613 1 I 201602 20160509 20160517 20160517 PER US-CELGENEUS-USA-2016052360 CELGENE 51.76 YR F Y 83.99000 KG 20160517 CN 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
123766131 12376613 1 PS ABRAXANE PACLITAXEL 1 Intravenous drip U UNKNOWN 21660 INJECTION FOR INFUSION
123766131 12376613 2 C LUPRON LEUPROLIDE ACETATE 1 Unknown 0 UNKNOWN /month
123766131 12376613 3 C ZOMETA ZOLEDRONIC ACID 1 Unknown 0 UNKNOWN
123766131 12376613 4 C THYROID SUPPLEMENT 2 Unknown 0 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123766131 12376613 1 Breast cancer metastatic
123766131 12376613 2 Product used for unknown indication
123766131 12376613 3 Bone disorder
123766131 12376613 4 Supplementation therapy

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
123766131 12376613 Generalised oedema
123766131 12376613 White blood cell disorder

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
123766131 12376613 1 201512 201604 0