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
5119567 6145293 I 5119567-3 20030528 20060919 20060929 EXP 2006112658 PFIZER INC. 70 YR M N 67.7 KG 20060928 UNITED STATES

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
5119567 1007725045 PS VORICONAZOLE (VORICONAZOLE) 2 U U 21266
5119567 1007749369 SS ALL OTHER THERAPEUTIC PRODUCTS (ALL OTHER THERAPEUTIC PRODUCTS) 2 ORAL 1200 MG, ORAL Y D
5119567 1007749375 C NORFLOXACIN 1
5119567 1007749381 C VALACYCLOVIR 1
5119567 1007749387 C GATIFLOXACIN 1
5119567 1007749393 C ALLOPURINOL 1
5119567 1007749394 C ATENOLOL 1
5119567 1007749395 C LEVAQUIN 1
5119567 1007749396 C PREDNISONE TAB 1
5119567 1007749397 C VALTREX 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
5119567 1007725045 DRUG USE FOR UNKNOWN INDICATION
5119567 1007749369 ACUTE MYELOID LEUKAEMIA

Outcome of event

Event ID OUTC COD
5119567 HO

Reactions reported

Event ID PT
5119567 ATRIAL FIBRILLATION
5119567 CATHETER RELATED COMPLICATION
5119567 HEPATOTOXICITY
5119567 HYPERNATRAEMIA
5119567 HYPOKALAEMIA
5119567 INDURATION
5119567 RENAL IMPAIRMENT

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

Event ID RPSR COD
5119567 HP

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
5119567 1007749369 20030513 20030528