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
126006461 12600646 1 I 20160719 20160727 20160727 EXP US-ALLERGAN-1663993US ALLERGAN 15.00 YR M Y 71.60000 KG 20160727 CN US US

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
126006461 12600646 1 PS BOTOX ONABOTULINUMTOXINA 1 Intramuscular 200 UNITS, SINGLE 103000 POWDER FOR INJECTION QD
126006461 12600646 2 SS BOTOX ONABOTULINUMTOXINA 1 Intramuscular 400 UNITS, SINGLE 103000 POWDER FOR INJECTION QD
126006461 12600646 3 SS BOTOX ONABOTULINUMTOXINA 1 Intramuscular 400 UNITS, SINGLE 103000 POWDER FOR INJECTION QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126006461 12600646 1 Hemiplegia

Outcome of event

Event ID CASEID OUTC COD
126006461 12600646 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126006461 12600646 Depression
126006461 12600646 Fatigue
126006461 12600646 Off label use
126006461 12600646 Pneumonia mycoplasmal
126006461 12600646 Somnolence
126006461 12600646 Suicidal ideation
126006461 12600646 Upper respiratory tract infection

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126006461 12600646 1 20120424 20120424 0
126006461 12600646 2 20131023 20131023 0
126006461 12600646 3 20160126 20160126 0