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
127914921 12791492 1 I 20160909 20160926 20160929 20160929 EXP US-CIPLA LTD.-2016US18916 CIPLA 0.00 Y 0.00000 20160929 CN 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
127914921 12791492 1 PS ESCITALOPRAM ESCITALOPRAM OXALATE 1 Oral 10 MG, QD 145 MG Y U 78604 10 MG TABLET QD
127914921 12791492 2 C TYLENOL ACETAMINOPHEN 1 Unknown UNK U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127914921 12791492 1 Generalised anxiety disorder
127914921 12791492 2 Headache

Outcome of event

Event ID CASEID OUTC COD
127914921 12791492 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127914921 12791492 Contact lens acute red eye
127914921 12791492 Disturbance in attention
127914921 12791492 Feeling abnormal
127914921 12791492 Headache
127914921 12791492 Insomnia
127914921 12791492 Ocular discomfort

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
127914921 12791492 1 20160826 20160921 0