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
4302897 4099502 I 4302897-2 20040219 20040223 DIR 72 YR M N 77.7 KG 20040220 OT N N

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
4302897 1004646566 PS GEMCITABINE 2 INTRAVENOUS 35-17 -5MG/M2 BIWEEKLY INTRAVENOUS D D
4302897 1004658602 C ASPIRIN 1
4302897 1004658603 C TIMOLOL MALEATE 1
4302897 1004658604 C NIACIN 1
4302897 1004658605 C ATORVASTATIN 2
4302897 1004658606 C FOSINOPRIL SODIUM 1
4302897 1004658607 C METOPROLOL 2
4302897 1004658608 C CARAFATE 1
4302897 1004658610 C DOCUSATE 2
4302897 1004658611 SS EXTERNAL BEAM RADIATION 2 OTHER 200CGY DAILY OTHER D D
4302897 1004669057 C ENSURE 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
4302897 1004646566 NON-SMALL CELL LUNG CANCER STAGE IIIB
4302897 1004658611 NON-SMALL CELL LUNG CANCER STAGE IIIB

Outcome of event

Event ID OUTC COD
4302897 HO
4302897 LT
4302897 RI

Reactions reported

Event ID PT
4302897 ATRIAL FIBRILLATION
4302897 DYSPNOEA EXERTIONAL
4302897 HYPOAESTHESIA
4302897 HYPOTENSION
4302897 PERIPHERAL COLDNESS
4302897 PYREXIA
4302897 SENSATION OF HEAVINESS

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
4302897 1004646566 20040106 20040213
4302897 1004658611 20040106 20040213