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
110048169 11004816 9 F 20160907 20150409 20160920 EXP US-PFIZER INC-2015119053 PFIZER 69.00 YR M Y 83.00000 KG 20160920 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
110048169 11004816 1 PS SUTENT SUNITINIB MALATE 1 50 MG CYCLIC 21938 50 MG CAPSULE, HARD
110048169 11004816 2 SS SUTENT SUNITINIB MALATE 1 37.5 MG CYCLIC (DAILY,28 DAYS ON /14 DAYS OFF) 21938 37.5 MG CAPSULE, HARD
110048169 11004816 3 SS SUTENT SUNITINIB MALATE 1 Oral 37.5 MG CYCLIC (28 DAYS ON /2 WEEKS OFF) (12.5MG THREE CAPSULES BY MOUTH ONCE IN THE MORNING) 082BA 21938 37.5 MG CAPSULE, HARD
110048169 11004816 4 C METFORMIN METFORMIN HYDROCHLORIDE 1 UNK 0
110048169 11004816 5 C GLIPIZIDE. GLIPIZIDE 1 UNK 0
110048169 11004816 6 C PRAVASTATIN. PRAVASTATIN 1 UNK 0
110048169 11004816 7 C LISINOPRIL. LISINOPRIL 1 UNK 0
110048169 11004816 8 C METOPROLOL. METOPROLOL 1 UNK 0
110048169 11004816 9 C MAGIC MOUTHWASH DIPHENHYDRAMINE HYDROCHLORIDELIDOCAINE HYDROCHLORIDENYSTATIN 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
110048169 11004816 1 Renal cancer metastatic
110048169 11004816 2 Renal cancer

Outcome of event

Event ID CASEID OUTC COD
110048169 11004816 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
110048169 11004816 Blister
110048169 11004816 Blood glucose increased
110048169 11004816 Drug prescribing error
110048169 11004816 Dry skin
110048169 11004816 Dysgeusia
110048169 11004816 Fatigue
110048169 11004816 Glossodynia
110048169 11004816 Hyperaesthesia
110048169 11004816 Musculoskeletal discomfort
110048169 11004816 Oral pain
110048169 11004816 Rash
110048169 11004816 Skin exfoliation
110048169 11004816 Skin hypertrophy
110048169 11004816 Skin reaction
110048169 11004816 Stomatitis
110048169 11004816 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
110048169 11004816 1 20150201 0
110048169 11004816 2 20150318 0
110048169 11004816 9 20150217 0