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
125389021 12538902 1 I 201302 20160624 20160708 20160708 EXP GB-TEVA-672099ACC TEVA 48.00 YR F Y 0.00000 20160708 MD GB GB

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
125389021 12538902 1 PS PACLITAXEL. PACLITAXEL 1 Unknown UNK, QWK U U 75297 /wk
125389021 12538902 2 SS PROLIA DENOSUMAB 1 Unknown UNK U 0
125389021 12538902 3 C CAPECITABINE. CAPECITABINE 1 0
125389021 12538902 4 C EVEROLIMUS EVEROLIMUS 1 0
125389021 12538902 5 C EXEMESTANE. EXEMESTANE 1 0
125389021 12538902 6 C LETROZOLE. LETROZOLE 1 0
125389021 12538902 7 C TAMOXIFEN TAMOXIFEN 1 0
125389021 12538902 8 C ZOLADEX GOSERELIN ACETATE 1 0
125389021 12538902 9 C ZOLEDRONIC ACID ZOLEDRONIC ACID 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125389021 12538902 1 Product used for unknown indication
125389021 12538902 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125389021 12538902 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125389021 12538902 Bone disorder
125389021 12538902 Breast cancer female
125389021 12538902 Cough
125389021 12538902 Disease progression
125389021 12538902 Lymphadenopathy mediastinal
125389021 12538902 Metastases to bone
125389021 12538902 Metastases to lymph nodes
125389021 12538902 Pericardial effusion
125389021 12538902 Pleural effusion
125389021 12538902 Pneumonitis

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

no results found

Therapies reported

no results found