The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
6194479 6867115 F 6194479-5 20080707 20090511 20090519 EXP PHHY2008JP32476 NOVARTIS PHARMACEUTICALS CORP. 69 F Y 48 KG 20090519 JAPAN

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
6194479 1011590890 PS ZOMETA 1 INTRAVENOUS 4 MG EVERY 4 WEEKS 21223
6194479 1011590891 SS AREDIA 1 INTRAVENOUS 60 MG EVERY 4 WEEKS
6194479 1011590892 SS TS 1 2 ORAL
6194479 1011590893 C ARTIST 2 ORAL
6194479 1011590894 C LIPITOR 1 ORAL
6194479 1011590895 C CONIEL 2 ORAL
6194479 1011590896 C RIZE 2 ORAL

Indications of drugs used

Event ID DRUG SEQ INDI PT
6194479 1011590890 METASTASES TO BONE
6194479 1011590891 METASTASES TO BONE
6194479 1011590892 LYMPH NODE CANCER METASTATIC

Outcome of event

Event ID OUTC COD
6194479 HO

Reactions reported

Event ID PT
6194479 ABSCESS
6194479 ABSCESS DRAINAGE
6194479 BONE DISORDER
6194479 DECUBITUS ULCER
6194479 GINGIVAL ERYTHEMA
6194479 GINGIVAL SWELLING
6194479 OSTEOMYELITIS
6194479 OSTEONECROSIS
6194479 PRIMARY SEQUESTRUM
6194479 SEQUESTRECTOMY
6194479 SWELLING

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6194479 1011590890 20060701 20080617
6194479 1011590891 20050101 20060601