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
121713233 12171323 3 F 201601 20160719 20160311 20160811 PER US-PFIZER INC-2016102007 PFIZER 62.00 YR F Y 0.00000 20160811 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
121713233 12171323 1 PS AZITHROMYCIN ANHYDROUS. AZITHROMYCIN ANHYDROUS 1 250 MG, UNK N 50711 250 MG FILM-COATED TABLET
121713233 12171323 2 SS AZITHROMYCIN ANHYDROUS. AZITHROMYCIN ANHYDROUS 1 250 MG, 1X/DAY (250 MG - 6 TABLETS ONE A DAY) N M39808 50711 1500 MG FILM-COATED TABLET QD
121713233 12171323 3 SS AZITHROMYCIN ANHYDROUS. AZITHROMYCIN ANHYDROUS 1 N 50711 FILM-COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121713233 12171323 1 Conjunctivitis
121713233 12171323 2 Dry eye
121713233 12171323 3 Ocular hyperaemia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
121713233 12171323 Dry eye
121713233 12171323 Product use issue

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
121713233 12171323 2 20160121 0