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
122799174 12279917 4 F 20151008 20160809 20160418 20160815 EXP US-ALLERGAN-1654015US ALLERGAN 62.00 YR F Y 0.00000 20160815 OT 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
122799174 12279917 1 PS BOTOX ONABOTULINUMTOXINA 1 Intramuscular UNK, SINGLE 103000 POWDER FOR INJECTION QD
122799174 12279917 2 SS BOTOX ONABOTULINUMTOXINA 1 Intramuscular UNK 103000 POWDER FOR INJECTION QD
122799174 12279917 3 C ADVIL IBUPROFEN 1 Oral UNK U 0
122799174 12279917 4 C TYLENOL ACETAMINOPHEN 1 Oral UNK U 0
122799174 12279917 5 C PHENERGAN PROMETHAZINE HYDROCHLORIDE 1 Oral UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122799174 12279917 1 Migraine
122799174 12279917 3 Pain
122799174 12279917 4 Pain
122799174 12279917 5 Pain

Outcome of event

Event ID CASEID OUTC COD
122799174 12279917 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
122799174 12279917 Anxiety
122799174 12279917 Chest discomfort
122799174 12279917 Dysphonia

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
122799174 12279917 1 20160114 20160114 0
122799174 12279917 2 20151008 20151008 0