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
127815531 12781553 1 I 20160815 20160823 20160926 20160926 EXP GB-ALLERGAN-1666676US ALLERGAN 41.00 YR F Y 0.00000 20160926 OT 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
127815531 12781553 1 PS BOTOX ONABOTULINUMTOXINA 1 Intradermal 62.5 UNITS, SINGLE D C4025 103000 POWDER FOR INJECTION QD
127815531 12781553 2 SS BOTOX ONABOTULINUMTOXINA 1 Intradermal 62.5 UNITS, SINGLE D 103000 POWDER FOR INJECTION QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127815531 12781553 1 Hyperhidrosis

Outcome of event

Event ID CASEID OUTC COD
127815531 12781553 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127815531 12781553 Blood pressure increased
127815531 12781553 Cerebrovascular accident
127815531 12781553 Dizziness
127815531 12781553 Muscular weakness
127815531 12781553 Off label use

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
127815531 12781553 1 20160812 20160812 0
127815531 12781553 2 20160812 20160812 0