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
112231603 11223160 3 F 20140905 20160812 20150626 20160817 EXP DK-DKMA-EFO12349 DK-ALLERGAN-1511829US ALLERGAN 45.00 YR F Y 50.00000 KG 20160817 CN DK DK

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
112231603 11223160 1 PS BOTOX ONABOTULINUMTOXINA 1 Intramuscular 55 UNITS, SINGLE 103000 POWDER FOR INJECTION QD
112231603 11223160 2 C LEVAXIN LEVOTHYROXINE SODIUM 1 U 0
112231603 11223160 3 C ETALPHA ALFACALCIDOL 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
112231603 11223160 1 Skin cosmetic procedure
112231603 11223160 2 Myxoedema
112231603 11223160 3 Calcium metabolism disorder

Outcome of event

Event ID CASEID OUTC COD
112231603 11223160 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
112231603 11223160 Anxiety
112231603 11223160 Confusional state
112231603 11223160 Dizziness
112231603 11223160 Dry eye
112231603 11223160 Dry mouth
112231603 11223160 Ear discomfort
112231603 11223160 Headache
112231603 11223160 Memory impairment
112231603 11223160 Nervous system disorder
112231603 11223160 Strabismus
112231603 11223160 Visual impairment

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
112231603 11223160 1 20140905 20140905 0
112231603 11223160 2 20100120 0
112231603 11223160 3 20100120 0