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
120945312 12094531 2 F 20160128 20160219 20160701 EXP US-APOTEX-2015AP015367 APOTEX 0.00 F Y 0.00000 20160701 OT 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
120945312 12094531 1 PS TIMOLOL MALEATE OPHTHALMIC SOLUTION USP TIMOLOL MALEATE 1 Ophthalmic 1 DROP IN EACH EYE IN THE MORNING, AND 1 DROP IN EACH EYE AT NIGHT N NDW4082 204936 EYE DROPS, SOLUTION BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
120945312 12094531 1 Glaucoma

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
120945312 12094531 Conjunctivitis viral
120945312 12094531 Eye infection viral
120945312 12094531 Lacrimation increased
120945312 12094531 Product contamination

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
120945312 12094531 1 20151212 0