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
126102821 12610282 1 I 20160726 20160801 20160801 EXP BR-PFIZER INC-2016364219 PFIZER 85.00 YR F Y 48.00000 KG 20160801 CN BR BR

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
126102821 12610282 1 PS XALATAN LATANOPROST 1 Ophthalmic 3 UG (ONE DROP IN EACH EYE), UNK U 51597 L44855 20597 3 UG EYE DROPS, SOLUTION
126102821 12610282 2 C AZOPT BRINZOLAMIDE 1 Ophthalmic 3 UG (ONE DROP IN EACH EYE), 2X/DAY (IN THE MORNING AND AT NIGHT) 62241 0 3 UG BID
126102821 12610282 3 C LACRIFILM CARBOXYMETHYLCELLULOSE SODIUM 1 Ophthalmic UNK, 4X/DAY 0 QID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126102821 12610282 1 Glaucoma
126102821 12610282 2 Glaucoma
126102821 12610282 3 Glaucoma

Outcome of event

Event ID CASEID OUTC COD
126102821 12610282 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126102821 12610282 Disturbance in attention
126102821 12610282 Nervousness
126102821 12610282 Visual acuity reduced
126102821 12610282 Weight decreased

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
126102821 12610282 1 2011 0
126102821 12610282 2 2011 0
126102821 12610282 3 2014 0