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
4466789 4200802 F 2 4466789-0 20040730 20040917 20040930 EXP HQWYE231012AUG04 WYETH LABS (RA) 56 YR M N 65.83 KG 20040929 MD

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
4466789 1005268352 PS RAPAMUNE 1 ORAL 5 MG 1X PER 1 DAY, ORAL D D 21083
4466789 1005288182 C PREDNISONE 1
4466789 1005288184 C SANDIMMUNE 1
4466789 1005288185 C HUMULIN (INSULIN HUMAN) 2
4466789 1005288186 C LOPRESSOR 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
4466789 1005268352 PROPHYLAXIS AGAINST TRANSPLANT REJECTION

Outcome of event

Event ID OUTC COD
4466789 HO

Reactions reported

Event ID PT
4466789 ABDOMINAL ABSCESS
4466789 BACTEROIDES INFECTION
4466789 BLOOD CREATININE INCREASED
4466789 CANDIDIASIS
4466789 EPSTEIN-BARR VIRUS ANTIBODY POSITIVE
4466789 ESCHERICHIA INFECTION
4466789 HAEMATOCRIT DECREASED
4466789 HAEMOGLOBIN DECREASED
4466789 ILEAL PERFORATION
4466789 INTESTINAL PERFORATION
4466789 PLATELET COUNT INCREASED
4466789 STAPHYLOCOCCAL INFECTION
4466789 STREPTOCOCCAL ABSCESS

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

Event ID RPSR COD
4466789 HP

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
4466789 1005268352 20040728 20040730