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
100120812 10012081 2 F 20140327 20140314 20140331 EXP GB-PFIZER INC-2014067797 PFIZER 0.00 M Y 0.00000 20140331 N CN GB GB

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
100120812 10012081 1 PS FLUCONAZOLE 1 U 19949
100120812 10012081 2 C BECLOMETASONE DIPROPIONATE 1 UNK D 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
100120812 10012081 1 Oral candidiasis
100120812 10012081 2 Asthma

Outcome of event

Event ID CASEID OUTC COD
100120812 10012081 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
100120812 10012081 Asthenia
100120812 10012081 Decreased appetite
100120812 10012081 Dehydration
100120812 10012081 Weight decreased

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

no results found

Therapies reported

no results found