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
126510121 12651012 1 I 20160602 0 20160812 20160812 DIR 29.00 YR F N 116.00000 LBS 20160811 N 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
126510121 12651012 1 PS BOTOX ONABOTULINUMTOXINA 1 N D 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126510121 12651012 1 Skin wrinkling

Outcome of event

Event ID CASEID OUTC COD
126510121 12651012 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126510121 12651012 Arthralgia
126510121 12651012 Asthenia
126510121 12651012 Blepharospasm
126510121 12651012 Chest discomfort
126510121 12651012 Dizziness
126510121 12651012 Dry eye
126510121 12651012 Eyelid ptosis
126510121 12651012 Fatigue
126510121 12651012 Headache
126510121 12651012 Memory impairment
126510121 12651012 Slow speech

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
126510121 12651012 1 20160325 0