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
123698873 12369887 3 F 20160228 20160627 20160516 20160701 EXP NZ-ALLERGAN-1656588US ALLERGAN 46.00 YR F Y 0.00000 20160630 OT COUNTRY NOT SPECIFIED NZ

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
123698873 12369887 1 PS BOTOX ONABOTULINUMTOXINA 1 Intramuscular 16 UNITS, SINGLE C3941 103000 POWDER FOR INJECTION QD
123698873 12369887 2 SS BOTOX ONABOTULINUMTOXINA 1 Intramuscular 6 UNITS, SINGLE 103000 POWDER FOR INJECTION QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123698873 12369887 1 Skin wrinkling
123698873 12369887 2 Skin wrinkling

Outcome of event

Event ID CASEID OUTC COD
123698873 12369887 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123698873 12369887 Anxiety
123698873 12369887 Cardiac disorder
123698873 12369887 Chest discomfort
123698873 12369887 Dyspnoea
123698873 12369887 Fatigue
123698873 12369887 Headache
123698873 12369887 Inflammation
123698873 12369887 Influenza like illness
123698873 12369887 Insomnia
123698873 12369887 Palpitations
123698873 12369887 Panic attack
123698873 12369887 Paraesthesia
123698873 12369887 Product preparation error

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
123698873 12369887 1 20160225 20160225 0
123698873 12369887 2 20160225 20160225 0