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
100200333 10020033 3 F 201312 20140623 20140318 20140630 EXP US-ALLERGAN-1404830US ALLERGAN 89.00 YR F Y 60.32000 KG 20140630 N MD 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
100200333 10020033 1 PS Alphagan P 1 OPHTHALMIC 1 GTT, BID IN LEFT EYE D 81637 21262 1 GTT EYE DROPS, SOLUTION BID
100200333 10020033 2 C ARTIFICIAL TEARS /00445101/ 2 U 0
100200333 10020033 3 C AMLODIPINE BESYLATE 1 U 0
100200333 10020033 4 C POTASSIUM 1 U 0
100200333 10020033 5 C TRIAMTERENE/HCTZ 1 U 0
100200333 10020033 6 C LEVOTHYROXINE 1 U 0
100200333 10020033 7 C TYLENOL 1 PRN U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
100200333 10020033 1 Normal tension glaucoma

Outcome of event

Event ID CASEID OUTC COD
100200333 10020033 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
100200333 10020033 Amnesia
100200333 10020033 Anxiety
100200333 10020033 Dysarthria
100200333 10020033 Inappropriate schedule of drug administration
100200333 10020033 Mental impairment

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
100200333 10020033 1 20131211 20140310 0