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
4464079 4223054 I 4464079-3 20040927 20040930 DIR M N 66 KG 20040930 OT 20040927 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
4464079 1005256157 PS GEMCITABINE 2 INTRAVENOUS 1000MG/M2, WKLY, IV D D
4464079 1005268205 C SPIRONOLACTONE 1
4464079 1005268206 C TEQUIN 1
4464079 1005268207 C OXYCODONE HCL 1
4464079 1005268208 C ATIVAN 1
4464079 1005268210 C HALDOL 1
4464079 1005268211 C RITALIN 1
4464079 1005268213 C REGLAN 1
4464079 1005268214 C PROTONIX 1
4464079 1005268215 C MIRALAX 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
4464079 1005256157 PANCREATIC CARCINOMA

Outcome of event

Event ID OUTC COD
4464079 DE

Reactions reported

Event ID PT
4464079 GENERAL PHYSICAL HEALTH DETERIORATION
4464079 PANCREATIC CARCINOMA
4464079 PERFORMANCE STATUS DECREASED
4464079 PNEUMONIA

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
4464079 1005256157 20040806 20040910