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
115869007 11586900 7 F 20150918 20160715 20151001 20160802 PER US-PFIZER INC-2015315767 PFIZER 69.00 YR F Y 64.00000 KG 20160802 MD 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
115869007 11586900 1 PS SUTENT SUNITINIB MALATE 1 Oral 37.5 MG, 1X/DAY Y X731B 21938 37.5 MG CAPSULE, HARD QD
115869007 11586900 2 SS SUTENT SUNITINIB MALATE 1 Oral 37.5 MG, 1X/DAY Y 258CA 21938 37.5 MG CAPSULE, HARD QD
115869007 11586900 3 C SANDOSTATIN OCTREOTIDE ACETATE 1 UNK 0 INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
115869007 11586900 1 Pancreatic neuroendocrine tumour metastatic
115869007 11586900 2 Pancreatic carcinoma

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
115869007 11586900 Alanine aminotransferase increased
115869007 11586900 Alopecia
115869007 11586900 Aspartate aminotransferase increased
115869007 11586900 Blood glucose decreased
115869007 11586900 Blood glucose fluctuation
115869007 11586900 Dry skin
115869007 11586900 Fatigue
115869007 11586900 Tooth disorder

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
115869007 11586900 1 20150820 0
115869007 11586900 2 20150820 0