The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
127616421 12761642 1 I 20160908 20160920 20160920 EXP GB-BAUSCH-BL-2016-022700 BAUSCH AND LOMB JONES N. SEPSIS DURING IMMUNOSUPPRESSION FOR SIGHT-THREATENING UVEITIS: THE FLIP SIDE. OCULAR IMMUNOLOGY AND INFLAMMATION. 2016;1-4. 61.00 YR M Y 0.00000 20160920 MD GB GB

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
127616421 12761642 1 PS MYCOPHENOLATE MOFETIL. MYCOPHENOLATE MOFETIL 1 Unknown Y 0 2.5 G
127616421 12761642 2 SS PREDNISOLONE. PREDNISOLONE 1 Unknown U 0 1.5 MG/KG
127616421 12761642 3 SS PREDNISOLONE. PREDNISOLONE 1 Unknown 40-60 MG U 0
127616421 12761642 4 SS PREDNISOLONE. PREDNISOLONE 1 Unknown U 0 40 MG
127616421 12761642 5 SS PREDNISOLONE. PREDNISOLONE 1 Unknown U 0 20 MG
127616421 12761642 6 SS INFLIXIMAB INFLIXIMAB 1 Unknown Y 0 5 MG/KG INFUSION
127616421 12761642 7 SS INFLIXIMAB INFLIXIMAB 1 Unknown INTRODUCED AT WEEKS 0, 2, AND 6, AND 8-WEEKLY THEREAFTER Y 0 5 MG/KG
127616421 12761642 8 C TRIMETHOPRIM/SULFAMETHOXAZOLE SULFAMETHOXAZOLETRIMETHOPRIM 1 0 480 MG TIW
127616421 12761642 9 C METHYLPREDNISOLONE. METHYLPREDNISOLONE 1 Intravenous (not otherwise specified) 3X1 G 0 QOW
127616421 12761642 10 C TRIAMCINOLONE TRIAMCINOLONE 1 Ophthalmic 0
127616421 12761642 11 C AZATHIOPRINE. AZATHIOPRINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127616421 12761642 1 Immunosuppression
127616421 12761642 2 Uveitis
127616421 12761642 6 Uveitis
127616421 12761642 8 Lymphopenia
127616421 12761642 9 Uveitis
127616421 12761642 10 Product used for unknown indication
127616421 12761642 11 Uveitis

Outcome of event

Event ID CASEID OUTC COD
127616421 12761642 HO
127616421 12761642 LT
127616421 12761642 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127616421 12761642 Intestinal obstruction
127616421 12761642 Multiple organ dysfunction syndrome
127616421 12761642 Pneumonia
127616421 12761642 Sepsis

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

no results found

Therapies reported

no results found