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
122670793 12267079 3 F 20160719 20160414 20160802 EXP US-PFIZER INC-2016195154 PFIZER 66.00 YR F Y 96.00000 KG 20160802 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
122670793 12267079 1 PS SUTENT SUNITINIB MALATE 1 50 MG, CYCLIC (4 CAPSULES DAILY 12.5MG, 28 DAYS ON/14 DAYS OFF) Y Z625A 21938 50 MG CAPSULE, HARD
122670793 12267079 2 C HYDROCODONE BITARTRATE AND ACETAMINOPHEN ACETAMINOPHENHYDROCODONE BITARTRATE 1 UNK 0
122670793 12267079 3 C METOPROLOL. METOPROLOL 1 UNK 0
122670793 12267079 4 C COZAAR LOSARTAN POTASSIUM 1 UNK 0
122670793 12267079 5 C XANAX ALPRAZOLAM 1 UNK 0
122670793 12267079 6 C FOLIC ACID. FOLIC ACID 1 UNK 0
122670793 12267079 7 C NAPROXEN. NAPROXEN 1 UNK, AS NEEDED 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122670793 12267079 1 Renal cell carcinoma
122670793 12267079 2 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
122670793 12267079 HO
122670793 12267079 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
122670793 12267079 Arthralgia
122670793 12267079 Chapped lips
122670793 12267079 Cyst
122670793 12267079 Dry mouth
122670793 12267079 Dry skin
122670793 12267079 Dyspepsia
122670793 12267079 Dysphagia
122670793 12267079 Erythema
122670793 12267079 Fatigue
122670793 12267079 Furuncle
122670793 12267079 Gingival discomfort
122670793 12267079 Haemorrhage
122670793 12267079 Hypersomnia
122670793 12267079 Lip haemorrhage
122670793 12267079 Oral discomfort
122670793 12267079 Oropharyngeal pain
122670793 12267079 Pain
122670793 12267079 Palmar-plantar erythrodysaesthesia syndrome
122670793 12267079 Rash
122670793 12267079 Swelling face
122670793 12267079 Tongue discomfort
122670793 12267079 Weight increased

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
122670793 12267079 1 20160314 0