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
104843847 10484384 7 F 2012 20160729 20140930 20160810 PER US-PFIZER INC-2014267227 PFIZER 53.00 YR M Y 98.00000 KG 20160810 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
104843847 10484384 1 PS SUTENT SUNITINIB MALATE 1 Oral 50 MG, CYCLIC (ONCE A DAY, 28 DAYS ON WASH OUT PERIOD AND TWO WEEKS OFF WASH OUT PERIOD) U X823B 21938 50 MG CAPSULE, HARD
104843847 10484384 2 SS SUTENT SUNITINIB MALATE 1 20 MG, CYCLIC (28 DAY ON 14 OFF) U 21938 20 MG CAPSULE, HARD
104843847 10484384 3 C VITAMIN C ASCORBIC ACID 1 Oral 1000 MG, 1X/DAY 0 1000 MG TABLET QD
104843847 10484384 4 C VITAMIN D CHOLECALCIFEROL 1 UNK 0
104843847 10484384 5 C PROPRANOLOL PROPRANOLOLPROPRANOLOL HYDROCHLORIDE 1 UNK 0
104843847 10484384 6 C TAMSULOSIN TAMSULOSIN 1 0.4 MG, UNK 0 .4 MG
104843847 10484384 7 C ESZOPICLONE. ESZOPICLONE 1 3 MG, UNK 0 3 MG
104843847 10484384 8 C VITAMIN D2 ERGOCALCIFEROL 1 Oral 50000 IU, WEEKLY 0 50000 IU CAPSULE /wk
104843847 10484384 9 C ASPIR 81 2 Oral 81 MG, 1X/DAY 0 81 MG PROLONGED-RELEASE TABLET QD
104843847 10484384 10 C BETA CAROTENE 2 Oral 30 MG, 1X/DAY 0 30 MG CAPSULE QD
104843847 10484384 11 C CENTRUM Complete 2 Oral UNK UNK, 1X/DAY, (18 MG 400 MCG TABLET) 0 TABLET QD
104843847 10484384 12 C LOMOTIL ATROPINE SULFATEDIPHENOXYLATE HYDROCHLORIDE 1 Oral UNK, (DIPHENOXYLATE HYDROCHLORIDE: 2.5 MG-ATROPINE SULFATE: 0.025 MG) 0 TABLET
104843847 10484384 13 C VITAMIN B12 CYANOCOBALAMIN 1 UNK 0
104843847 10484384 14 C VITAMIN B-6 PYRIDOXINE 1 UNK 0
104843847 10484384 15 C VITAMIN E .ALPHA.-TOCOPHEROL 1 UNK 0
104843847 10484384 16 C ZANTAC RANITIDINE HYDROCHLORIDE 1 Oral 150 MG, 1X/DAY (AT BED TIME HS) 0 150 MG TABLET QD
104843847 10484384 17 C XANAX ALPRAZOLAM 1 Oral 1 MG, AS NEEDED (AT BEDTIME (HS) PRN) 0 1 MG TABLET
104843847 10484384 18 C XGEVA DENOSUMAB 1 UNK UNK, CYCLIC (Q4 WK X 3 CYCLES X 1.0) 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
104843847 10484384 1 Metastatic renal cell carcinoma
104843847 10484384 7 Sleep disorder
104843847 10484384 17 Sleep disorder
104843847 10484384 18 Renal cancer

Outcome of event

Event ID CASEID OUTC COD
104843847 10484384 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
104843847 10484384 Back pain
104843847 10484384 Constipation
104843847 10484384 Contusion
104843847 10484384 Delusion
104843847 10484384 Diarrhoea
104843847 10484384 Dyspnoea
104843847 10484384 Faeces discoloured
104843847 10484384 Faeces pale
104843847 10484384 Fatigue
104843847 10484384 Gastrooesophageal reflux disease
104843847 10484384 Gingival bleeding
104843847 10484384 Hair colour changes
104843847 10484384 Hypoaesthesia
104843847 10484384 Impaired healing
104843847 10484384 Insomnia
104843847 10484384 Irritability
104843847 10484384 Muscle spasms
104843847 10484384 Muscle twitching
104843847 10484384 Pain in jaw
104843847 10484384 Paraesthesia
104843847 10484384 Pruritus
104843847 10484384 Thinking abnormal
104843847 10484384 Visual impairment
104843847 10484384 Yellow skin

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
104843847 10484384 1 201209 0
104843847 10484384 2 201209 0
104843847 10484384 3 2012 0
104843847 10484384 4 2011 0
104843847 10484384 6 2011 0
104843847 10484384 7 2012 0
104843847 10484384 8 2011 0
104843847 10484384 18 20130109 20130306 0