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
127543711 12754371 1 I 20160909 20160916 20160916 EXP PHEH2016US023001 NOVARTIS 0.00 M Y 0.00000 20160916 OT 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
127543711 12754371 1 PS ZOMETA ZOLEDRONIC ACID 1 Unknown UNK 21223
127543711 12754371 2 SS SUTENT SUNITINIB MALATE 1 Unknown 50 MG, 2 WEEKS ON/ 1 WEEK OFF U 0 50 MG
127543711 12754371 3 C MULTI VIT 2 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127543711 12754371 1 Metastatic renal cell carcinoma
127543711 12754371 2 Metastatic renal cell carcinoma
127543711 12754371 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127543711 12754371 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127543711 12754371 Bone neoplasm
127543711 12754371 Decreased appetite
127543711 12754371 Dry mouth
127543711 12754371 Fatigue
127543711 12754371 Musculoskeletal chest pain
127543711 12754371 Pain
127543711 12754371 Upper limb fracture
127543711 12754371 White blood cell count decreased

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
127543711 12754371 2 20160629 0