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
127134983 12713498 3 F 20160909 20160903 20160916 EXP US-AMGEN-USASP2016116530 AMGEN 0.00 F Y 0.00000 20160916 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
127134983 12713498 1 PS NEULASTA PEGFILGRASTIM 1 Unknown UNK U 125031 UNKNOWN FORMULATION
127134983 12713498 2 SS TAXOL PACLITAXEL 1 Unknown UNK 0
127134983 12713498 3 C ADRIAMYCIN DOXORUBICIN HYDROCHLORIDE 1 UNK 0
127134983 12713498 4 C CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 UNK 0
127134983 12713498 5 C AROMASIN EXEMESTANE 1 UNK 0
127134983 12713498 6 C TAMOXIFEN TAMOXIFEN 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127134983 12713498 1 Product used for unknown indication
127134983 12713498 2 Breast cancer
127134983 12713498 3 Breast cancer
127134983 12713498 4 Breast cancer
127134983 12713498 5 Breast cancer
127134983 12713498 6 Breast cancer

Outcome of event

Event ID CASEID OUTC COD
127134983 12713498 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127134983 12713498 Back pain
127134983 12713498 Breast cancer
127134983 12713498 Breast pain
127134983 12713498 Hypersensitivity
127134983 12713498 Metastases to lymph nodes
127134983 12713498 Ovarian cyst
127134983 12713498 Renal tumour excision
127134983 12713498 Unevaluable event

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found