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
126255571 12625557 1 I 20130621 20160805 20160805 EXP GB-PFIZER INC-2013177586 ALCN2013GB002415 SANDOZ 71.00 YR F Y 0.00000 20160805 OT 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
126255571 12625557 1 SS AZOPT BRINZOLAMIDE 1 Ophthalmic UNK U UNKNOWN 0
126255571 12625557 2 PS TIMOLOL. TIMOLOL 1 Ophthalmic UNK U U UNKNOWN 72550 EYE DROPS NOS
126255571 12625557 3 SS ALPHAGAN P BRIMONIDINE TARTRATE 1 Ophthalmic UNK U UNKNOWN 0
126255571 12625557 4 SS COSOPT DORZOLAMIDE HYDROCHLORIDETIMOLOL MALEATE 1 Ophthalmic 1 DF, BID U UNKNOWN 0 1 DF BID
126255571 12625557 5 SS TRUSOPT DORZOLAMIDE HYDROCHLORIDE 1 Ophthalmic UNK U UNKNOWN 0
126255571 12625557 6 SS XALATAN LATANOPROST 1 Ophthalmic 1 DF, QD U UNKNOWN 0 1 DF QD
126255571 12625557 7 C Amitriptyline AMITRIPTYLINE 1 Oral 10 MG, QD U UNKNOWN 0 10 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126255571 12625557 1 Glaucoma
126255571 12625557 2 Glaucoma
126255571 12625557 3 Glaucoma
126255571 12625557 4 Glaucoma
126255571 12625557 5 Glaucoma
126255571 12625557 6 Glaucoma
126255571 12625557 7 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126255571 12625557 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126255571 12625557 Condition aggravated
126255571 12625557 Drug ineffective
126255571 12625557 Glaucoma

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

no results found

Therapies reported

no results found