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
125467951 12546795 1 I 20160204 20160711 20160711 PER US-TEVA-633019USA TEVA 0.00 F Y 71.73000 KG 20160711 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
125467951 12546795 1 PS VENLAFAXINE VENLAFAXINE HYDROCHLORIDE 1 Oral IN THE MORNING U 76565 150 MG
125467951 12546795 2 SS VENLAFAXINE VENLAFAXINE HYDROCHLORIDE 1 U 76565
125467951 12546795 3 C CITALOPRAM HYDROBROMIDE. CITALOPRAM HYDROBROMIDE 1 20 MILLIGRAM DAILY; 0 20 MG QD
125467951 12546795 4 C SUDAFED PE CONGESTION PHENYLEPHRINE HYDROCHLORIDE 1 4 HOUR TABLET 0
125467951 12546795 5 C PROAIR HFA ALBUTEROL SULFATE 1 PRN HS FOR 30 YEARS 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125467951 12546795 1 Anxiety
125467951 12546795 2 Depression
125467951 12546795 4 Nasal congestion
125467951 12546795 5 Asthma

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125467951 12546795 Headache
125467951 12546795 Nightmare
125467951 12546795 Product substitution issue

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

no results found

Therapies reported

no results found