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
126764481 12676448 1 I 20160810 20160823 20160823 EXP IE-HPRA-2016-027413 IE-TEVA-684431ACC TEVA 0.00 F Y 0.00000 20160823 CN IE IE

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
126764481 12676448 1 PS ESCITALOPRAM ESCITALOPRAM OXALATE 1 Oral Y 76765 5 MG FILM-COATED TABLET
126764481 12676448 2 C Eltroxin LEVOTHYROXINE 1 50MG MON-FRI, 100MG SAT-SUN 0 50 MG TABLET
126764481 12676448 3 C Eltroxin LEVOTHYROXINE 1 50MG MON-FRI, 100MG SAT-SUN 0 100 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126764481 12676448 1 Depression

Outcome of event

Event ID CASEID OUTC COD
126764481 12676448 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126764481 12676448 Epistaxis
126764481 12676448 Feeling abnormal
126764481 12676448 Headache
126764481 12676448 Lethargy
126764481 12676448 Slow speech
126764481 12676448 Somnolence
126764481 12676448 Speech disorder
126764481 12676448 Thinking abnormal
126764481 12676448 Thirst

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

no results found

Therapies reported

no results found