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
125985162 12598516 2 F 201607 20160916 20160726 20160919 EXP US-ALLERGAN-1663793US ALLERGAN 57.00 YR F Y 40.82000 KG 20160919 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
125985162 12598516 1 PS BOTOX ONABOTULINUMTOXINA 1 Intramuscular 185 UNITS, SINGLE D 103000 POWDER FOR INJECTION QD
125985162 12598516 2 C GABAPENTIN. GABAPENTIN 1 UNK U 0
125985162 12598516 3 C GABAPENTIN. GABAPENTIN 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125985162 12598516 1 Torticollis
125985162 12598516 2 Fibromyalgia
125985162 12598516 3 Neuropathy peripheral

Outcome of event

Event ID CASEID OUTC COD
125985162 12598516 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125985162 12598516 Chronic obstructive pulmonary disease
125985162 12598516 Confusional state
125985162 12598516 Dysphagia
125985162 12598516 Fatigue
125985162 12598516 Feeding disorder
125985162 12598516 Feeling abnormal
125985162 12598516 Flushing
125985162 12598516 Hypersensitivity
125985162 12598516 Hypertension
125985162 12598516 Influenza like illness
125985162 12598516 Malaise
125985162 12598516 Palpitations
125985162 12598516 Paralysis
125985162 12598516 Presyncope
125985162 12598516 Skin burning sensation
125985162 12598516 Tremor
125985162 12598516 Vision blurred
125985162 12598516 Weight decreased

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
125985162 12598516 1 20160705 20160705 0