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
125744491 12574449 1 I 20160620 0 20160719 20160719 DIR 61.00 YR M N 58.60000 KG 20160712 N PH 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
125744491 12574449 1 PS LITHIUM. LITHIUM 1 Oral 0 300 MG QID
125744491 12574449 2 SS CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Oral 0 20 MG QD

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
125744491 12574449 HO
125744491 12574449 RI

Reactions reported

Event ID CASEID DRUG REC ACT PT
125744491 12574449 Blood pressure increased
125744491 12574449 Confusional state
125744491 12574449 Dehydration
125744491 12574449 Delirium
125744491 12574449 Diarrhoea
125744491 12574449 Ecchymosis
125744491 12574449 Hypercapnia
125744491 12574449 Movement disorder
125744491 12574449 Nausea
125744491 12574449 Respiratory failure
125744491 12574449 Serotonin syndrome
125744491 12574449 Sinus tachycardia
125744491 12574449 Tremor
125744491 12574449 Vomiting

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

Event ID CASEID RPSR COD
125744491 12574449 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
125744491 12574449 1 20060824 20160623 0
125744491 12574449 2 20061212 20160623 0