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
124162003 12416200 3 F 201512 20160809 20160530 20160819 EXP PE-PFIZER INC-2016271836 PFIZER 77.00 YR F Y 0.00000 20160819 CN PE PE

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
124162003 12416200 1 PS XALATAN LATANOPROST 1 UNK, AT NIGHTS U M38075|M78311|M79117 20597 EYE DROPS, SOLUTION QD
124162003 12416200 2 SS UNIAL HYALURONATE SODIUM 1 UNK, EVERY 8 HOURS U 0 TID
124162003 12416200 3 SS KRYTANTEK BRIMONIDINE TARTRATEDORZOLAMIDE HYDROCHLORIDETIMOLOL MALEATE 1 UNK, 2X/DAY U 0 BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124162003 12416200 1 Glaucoma

Outcome of event

Event ID CASEID OUTC COD
124162003 12416200 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124162003 12416200 Abasia
124162003 12416200 Osteoarthritis
124162003 12416200 Osteoporosis
124162003 12416200 Rheumatoid arthritis
124162003 12416200 Spinal disorder
124162003 12416200 Urinary tract infection
124162003 12416200 Visual impairment

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

no results found

Therapies reported

no results found