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
126632271 12663227 1 I 20160518 0 20160817 20160817 DIR 21.00 YR F N 125.00000 LBS 20160816 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
126632271 12663227 1 PS EPINEPHRINE. EPINEPHRINE 1 N D 0
126632271 12663227 2 C GENERESS FE ETHINYL ESTRADIOLFERROUS FUMARATENORETHINDRONE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126632271 12663227 1 Food allergy
126632271 12663227 1 Throat irritation

Outcome of event

Event ID CASEID OUTC COD
126632271 12663227 OT
126632271 12663227 DS
126632271 12663227 HO
126632271 12663227 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126632271 12663227 Anxiety
126632271 12663227 Apparent death
126632271 12663227 Blindness
126632271 12663227 Deafness
126632271 12663227 Myocardial infarction
126632271 12663227 Nausea
126632271 12663227 Vomiting

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
126632271 12663227 1 20160518 20160518 0