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
124797648 12479764 8 F 20160705 20160825 20160620 20160905 EXP US-PFIZER INC-2016285752 PFIZER 79.00 YR F Y 88.00000 KG 20160905 CN 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
124797648 12479764 1 PS SUTENT SUNITINIB MALATE 1 50 MG, UNK (2 WEEKS ON/1 WEEK OFF) Y 21938 50 MG CAPSULE, HARD
124797648 12479764 2 SS SUTENT SUNITINIB MALATE 1 37.5 MG, (2 WEEKS ON/1 WEEK OFF) Y 21938 37.5 MG CAPSULE, HARD
124797648 12479764 3 SS SUTENT SUNITINIB MALATE 1 37.5 MG, (2 WEEKS ON/1 WEEK OFF) Y 21938 37.5 MG CAPSULE, HARD
124797648 12479764 4 SS SUTENT SUNITINIB MALATE 1 37.5 MG, (2 WEEKS ON/1 WEEK OFF) Y 21938 37.5 MG CAPSULE, HARD
124797648 12479764 5 C METOPROLOL. METOPROLOL 1 UNK 0
124797648 12479764 6 C LIPITOR ATORVASTATIN CALCIUM 1 UNK 0
124797648 12479764 7 C VITAMIN D CHOLECALCIFEROL 1 UNK 0
124797648 12479764 8 C VITAMIN B VITAMIN B 1 UNK 0
124797648 12479764 9 C VITAMIN C ASCORBIC ACID 1 UNK 0
124797648 12479764 10 C CALCIUM CALCIUM 1 UNK 0
124797648 12479764 11 C POTASSIUM POTASSIUM 1 UNK 0
124797648 12479764 12 C SULFASALAZINE. SULFASALAZINE 1 UNK 0
124797648 12479764 13 C FLONASE FLUTICASONE PROPIONATE 1 UNK 0
124797648 12479764 14 C SINGULAIR MONTELUKAST SODIUM 1 UNK 0
124797648 12479764 15 C HYDRALAZINE HYDRALAZINE HYDROCHLORIDE 1 UNK 0
124797648 12479764 16 C PREVALITE CHOLESTYRAMINE 1 UNK, AS NEEDED 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124797648 12479764 1 Metastatic renal cell carcinoma
124797648 12479764 12 Crohn's disease
124797648 12479764 16 Abnormal faeces

Outcome of event

Event ID CASEID OUTC COD
124797648 12479764 OT
124797648 12479764 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124797648 12479764 Arthralgia
124797648 12479764 Asthenia
124797648 12479764 Blister
124797648 12479764 Blood pressure decreased
124797648 12479764 Conjunctivitis
124797648 12479764 Constipation
124797648 12479764 Decreased appetite
124797648 12479764 Diarrhoea
124797648 12479764 Dry mouth
124797648 12479764 Dry skin
124797648 12479764 Dysgeusia
124797648 12479764 Dyspepsia
124797648 12479764 Eye discharge
124797648 12479764 Faeces soft
124797648 12479764 Fatigue
124797648 12479764 Gastrointestinal haemorrhage
124797648 12479764 Haemorrhoids
124797648 12479764 Hypersensitivity
124797648 12479764 Hypertension
124797648 12479764 Incontinence
124797648 12479764 Kidney infection
124797648 12479764 Malaise
124797648 12479764 Memory impairment
124797648 12479764 Ocular hyperaemia
124797648 12479764 Pain in extremity
124797648 12479764 Peripheral swelling
124797648 12479764 Pruritus
124797648 12479764 Sinus disorder
124797648 12479764 Sleep disorder
124797648 12479764 Urinary tract infection
124797648 12479764 Weight 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
124797648 12479764 1 20160519 20160630 0
124797648 12479764 2 20160711 20160713 0
124797648 12479764 3 20160718 20160807 0
124797648 12479764 4 20160817 0
124797648 12479764 13 20160616 0
124797648 12479764 14 20160616 0
124797648 12479764 15 20160615 0