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
126072671 12607267 1 I 20160718 20160729 20160729 EXP AU-VERNALIS THERAPEUTICS, INC.-2016VRN00040 VERNALIS ZHAO C, DANIEL BS, MURRELL DF. DEBILITATING LATE OUTCOMES OF TOXIC EPIDERMAL NECROLYSIS (TEN): PRESENTATION OF TWO CASES. AUSTRALAS J DERMATOL. 2016;57:84 70.00 YR F Y 0.00000 20160728 OT AU AU

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
126072671 12607267 1 PS AMOXICILLIN. AMOXICILLIN 1 Unknown U 50813

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126072671 12607267 OT
126072671 12607267 HO
126072671 12607267 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
126072671 12607267 Activities of daily living impaired
126072671 12607267 Corneal disorder
126072671 12607267 Device related infection
126072671 12607267 Diarrhoea
126072671 12607267 Eye infection
126072671 12607267 Injury corneal
126072671 12607267 Photosensitivity reaction
126072671 12607267 Toxic epidermal necrolysis
126072671 12607267 Visual acuity reduced

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

no results found

Therapies reported

no results found