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
6024659 6870581 I 6024659-0 20060519 20081226 20081231 EXP JP-BRISTOL-MYERS SQUIBB COMPANY-14456321 BRISTOL-MYERS SQUIBB COMPANY 64 YR M Y 20081231 OT 20061004 JAPAN

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
6024659 1010940255 PS PARAPLATIN 1 INTRAVENOUS DRIP THERAPY STARTED FROM 16MAY06 19880
6024659 1010940256 SS TAXOTERE 1 INTRAVENOUS DRIP THERAPY STARTED FROM 16MAY06
6024659 1010940257 SS PICIBANIL 2 INTRAPLEURAL GIVEN ON 28AUG06(5KE,1DAY);ALSO ON 30AUG06,5SEP06,11SEP06 AND 21SEP06(10KE,4DAYS)
6024659 1010940258 C GASTER D 2 ORAL
6024659 1010940259 C EURODIN 2 ORAL
6024659 1010940260 C MAGLAX 2 ORAL
6024659 1010940261 C PREDONINE 2 ORAL
6024659 1010940262 C PURSENNID 2 ORAL

Indications of drugs used

Event ID DRUG SEQ INDI PT
6024659 1010940255 LUNG NEOPLASM MALIGNANT
6024659 1010940256 LUNG NEOPLASM MALIGNANT
6024659 1010940257 PNEUMOTHORAX

Outcome of event

Event ID OUTC COD
6024659 DE
6024659 HO
6024659 LT

Reactions reported

Event ID PT
6024659 INTERSTITIAL LUNG DISEASE
6024659 PNEUMOTHORAX

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
6024659 1010940255 20060718 20060718 4 DAY
6024659 1010940256 20060718 20060718 4 DAY
6024659 1010940257 20060828 20060921
6024659 1010940258 20060512 20060925
6024659 1010940259 20060608 20060925
6024659 1010940260 20060319 20060925
6024659 1010940261 20060601 20060925
6024659 1010940262 20060609 20060925