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
126148771 12614877 1 I 20160727 20160802 20160802 EXP FR-ALLERGAN-1664296US ALLERGAN 28.00 YR F Y 0.00000 20160802 OT FR FR

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
126148771 12614877 1 PS BOTOX ONABOTULINUMTOXINA 1 Intramuscular UNK, SINGLE 0 POWDER FOR INJECTION QD
126148771 12614877 2 C BACLOFENE BACLOFEN 1 UNK U 0
126148771 12614877 3 C MONTELUKAST MONTELUKAST SODIUM 1 UNK U 0
126148771 12614877 4 C OMEPRAZOLE. OMEPRAZOLE 1 UNK U 0
126148771 12614877 5 C DAILY ETHINYL ESTRADIOLLEVONORGESTREL 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126148771 12614877 1 Muscle spasticity

Outcome of event

Event ID CASEID OUTC COD
126148771 12614877 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126148771 12614877 Abnormal behaviour
126148771 12614877 Agitation
126148771 12614877 Anger
126148771 12614877 Depression
126148771 12614877 Malaise

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found