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
105256624 10525662 4 F 201512 20160712 20141017 20160715 EXP PHHY2014AR132278 NOVARTIS 54.56 YR F Y 0.00000 20160716 CN COUNTRY NOT SPECIFIED AR

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
105256624 10525662 1 PS AFINITOR EVEROLIMUS 1 Oral 10 MG, QD 22334 10 MG TABLET QD
105256624 10525662 2 SS AFINITOR EVEROLIMUS 1 Oral 10 MG, QD 22334 10 MG TABLET QD
105256624 10525662 3 C IBUPROFEN. IBUPROFEN 1 Unknown 0
105256624 10525662 4 C DICLOFENAC DICLOFENAC 1 Unknown 75 MG, UNK 0 75 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
105256624 10525662 1 Breast cancer
105256624 10525662 3 Product used for unknown indication
105256624 10525662 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
105256624 10525662 HO
105256624 10525662 OT
105256624 10525662 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
105256624 10525662 Anaemia
105256624 10525662 Bone pain
105256624 10525662 Calcium metabolism disorder
105256624 10525662 Dysstasia
105256624 10525662 Gait disturbance
105256624 10525662 Malignant neoplasm progression
105256624 10525662 Metastases to bone
105256624 10525662 Nosocomial infection
105256624 10525662 Pain in extremity
105256624 10525662 Post procedural complication

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
105256624 10525662 1 201406 201407 0
105256624 10525662 2 201407 0