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
8016625 8317514 I 8016625-0 20111222 20111231 EXP PHHY2011DE112455 SANDOZ,INC. 56 YR M Y 20111231 OT GERMANY

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
8016625 1018419900 SS CYCLOSPORINE 1 UNK
8016625 1018419901 PS MYCOPHENOLATE MOFETIL 1 UNK 065379
8016625 1018419902 SS MYCOPHENOLATE MOFETIL 1 UNK 065379
8016625 1018419903 SS STEROIDS NOS 2 UNK

Indications of drugs used

Event ID DRUG SEQ INDI PT
8016625 1018419900 IMMUNOSUPPRESSION
8016625 1018419901 IMMUNOSUPPRESSION

Outcome of event

Event ID OUTC COD
8016625 OT
8016625 DE

Reactions reported

Event ID PT
8016625 GASTRIC MUCOSAL LESION
8016625 EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER
8016625 SQUAMOUS CELL CARCINOMA

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

no results found

Therapies reported

no results found