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
125791912 12579191 2 F 201309 20160805 20160721 20160805 EXP TW-BAYER-2016-136787 BAYER 26.00 YR A F Y 0.00000 20160805 CN TW TW

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
125791912 12579191 1 PS NEXAVAR SORAFENIB 1 800 MG, QD 21923 800 MG FILM-COATED TABLET QD
125791912 12579191 2 C INTERFERON ALFA NOS INTERFERON ALFA-2A OR INTERFERON ALFA-2B 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125791912 12579191 1 Metastatic renal cell carcinoma
125791912 12579191 2 Metastatic renal cell carcinoma

Outcome of event

Event ID CASEID OUTC COD
125791912 12579191 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125791912 12579191 Asthenia
125791912 12579191 Cachexia
125791912 12579191 Conjunctivitis
125791912 12579191 Hyponatraemia
125791912 12579191 Metastases to lymph nodes
125791912 12579191 Metastases to skin
125791912 12579191 Mucosal inflammation
125791912 12579191 Palmar-plantar erythrodysaesthesia syndrome
125791912 12579191 Renal cell carcinoma stage IV
125791912 12579191 Somnolence
125791912 12579191 Vaginal infection

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
125791912 12579191 1 201308 201309 0
125791912 12579191 2 201307 0