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
125220272 12522027 2 F 201604 20160701 20160701 20160707 EXP TR-ALLERGAN-1655299US ALLERGAN 58.00 YR F Y 0.00000 20160707 MD COUNTRY NOT SPECIFIED TR

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
125220272 12522027 1 PS BOTOX ONABOTULINUMTOXINA 1 Intramuscular 50 UNITS, SINGLE 103000 POWDER FOR INJECTION QD
125220272 12522027 2 SS BOTOX ONABOTULINUMTOXINA 1 Intramuscular 50 UNITS, SINGLE 103000 POWDER FOR INJECTION QD
125220272 12522027 3 SS BOTOX ONABOTULINUMTOXINA 1 Intramuscular 50 UNITS, SINGLE 103000 POWDER FOR INJECTION QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125220272 12522027 1 Hyperhidrosis
125220272 12522027 2 Skin wrinkling
125220272 12522027 3 Skin wrinkling

Outcome of event

Event ID CASEID OUTC COD
125220272 12522027 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125220272 12522027 Aphasia
125220272 12522027 Eyelid ptosis
125220272 12522027 Gait disturbance
125220272 12522027 Malaise
125220272 12522027 Mastication disorder
125220272 12522027 Muscular weakness
125220272 12522027 Myasthenia gravis
125220272 12522027 Paraesthesia

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
125220272 12522027 1 201604 201604 0
125220272 12522027 2 201604 201604 0
125220272 12522027 3 201604 201604 0