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
6524173 7235365 I 6524173-X 20080101 20091222 20091231 EXP GB-WATSON-2009-11030 WATSON 21 YR M Y 20091231 OT UNITED KINGDOM

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
6524173 1012889275 PS HYDROCORTISONE ACETATE 1 INTRAVENOUS UNK UNCONFIRMED 083128
6524173 1012889276 SS HYDROCORTISONE ACETATE 1 RECTAL UNCONFIRMED 083128
6524173 1012889277 SS AZATHIOPRINE 1 100 MG, DAILY

Indications of drugs used

Event ID DRUG SEQ INDI PT
6524173 1012889275 COLITIS ULCERATIVE
6524173 1012889277 COLITIS ULCERATIVE

Outcome of event

Event ID OUTC COD
6524173 HO
6524173 OT

Reactions reported

Event ID PT
6524173 LEUKOPENIA
6524173 PNEUMOCYSTIS JIROVECI PNEUMONIA
6524173 PNEUMOMEDIASTINUM

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
6524173 1012889277 20050901 915 DAY