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
126956141 12695614 1 I 2015 20160309 20160829 20160829 PER US-KALEO, INC-2016SA050610 KALEO 0.00 F Y 0.00000 20160829 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
126956141 12695614 1 PS AUVI-Q EPINEPHRINE 1 TWICE IM OR SC 000002620206 201739 .3 MG
126956141 12695614 2 SS AUVI-Q EPINEPHRINE 1 000002620206 201739 .3 MG
126956141 12695614 3 SS EPINEPHRINE. EPINEPHRINE 1 UNKNOWN 0
126956141 12695614 4 SS STEROIDS UNSPECIFIED INGREDIENT 1 UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126956141 12695614 1 Hypersensitivity
126956141 12695614 3 Hypersensitivity
126956141 12695614 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126956141 12695614 Drug ineffective
126956141 12695614 Fluid retention
126956141 12695614 Oedema

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
126956141 12695614 1 20150704 201510 0
126956141 12695614 2 20151014 0
126956141 12695614 3 20151014 0
126956141 12695614 4 2015 0