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
127503342 12750334 2 F 20160921 20160916 20160928 PER US-PFIZER INC-2016433470 PFIZER 0.00 F Y 0.00000 20160928 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
127503342 12750334 1 PS DIFLUCAN FLUCONAZOLE 1 150 MG, UNK U 19949 150 MG
127503342 12750334 2 SS DIFLUCAN FLUCONAZOLE 1 200 MG, UNK U 19949 200 MG
127503342 12750334 3 SS DIFLUCAN FLUCONAZOLE 1 100 MG, UNK U 19949 100 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127503342 12750334 1 Candida infection
127503342 12750334 2 Oral candidiasis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127503342 12750334 Off label use
127503342 12750334 Oropharyngeal discomfort
127503342 12750334 Rebound effect
127503342 12750334 Tongue discolouration

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

no results found

Therapies reported

no results found