The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
5327956 6269792 F 5327956-7 20070312 20070507 20070517 EXP DE-PFIZER INC-2007020689 PFIZER INC F Y 58 KG 20070517 GERMANY

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
5327956 1008490648 PS SU-011,248 2 ORAL 21938
5327956 1008490649 SS GEMCITABINE 1 INTRAVENOUS
5327956 1008490650 SS CISPLATIN 1 INTRAVENOUS

Indications of drugs used

Event ID DRUG SEQ INDI PT
5327956 1008490648 NON-SMALL CELL LUNG CANCER
5327956 1008490649 NON-SMALL CELL LUNG CANCER
5327956 1008490650 NON-SMALL CELL LUNG CANCER

Outcome of event

Event ID OUTC COD
5327956 HO

Reactions reported

Event ID PT
5327956 ATRIAL THROMBOSIS
5327956 PULMONARY EMBOLISM
5327956 THROMBOSIS

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
5327956 1008490648 20061222 20070315