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
126902771 12690277 1 I 20160822 20160826 20160826 EXP BR-PFIZER INC-2016400006 PFIZER 0.00 F Y 0.00000 20160826 CN BR BR

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
126902771 12690277 1 PS PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 50 MG, 1X/DAY Y U 21992 50 MG PROLONGED-RELEASE TABLET QD
126902771 12690277 2 SS PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 100 MG, 1X/DAY Y U 21992 100 MG PROLONGED-RELEASE TABLET QD

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126902771 12690277 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126902771 12690277 Agitation
126902771 12690277 Anxiety
126902771 12690277 Chest discomfort
126902771 12690277 Condition aggravated
126902771 12690277 Crying
126902771 12690277 Decreased appetite
126902771 12690277 Depressed mood
126902771 12690277 Depression
126902771 12690277 Disorientation
126902771 12690277 Dyspnoea
126902771 12690277 Feeling abnormal
126902771 12690277 Headache
126902771 12690277 Increased appetite
126902771 12690277 Insomnia
126902771 12690277 Irritability
126902771 12690277 Malaise
126902771 12690277 Middle insomnia
126902771 12690277 Mydriasis
126902771 12690277 Neck pain
126902771 12690277 Suicidal ideation
126902771 12690277 Tachycardia
126902771 12690277 Tension
126902771 12690277 Tremor

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

no results found

Therapies reported

no results found