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
125564831 12556483 1 I 20160708 20160714 20160714 EXP US-PFIZER INC-2016338240 PFIZER 0.00 Y 0.00000 20160714 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
125564831 12556483 1 PS PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 50 MG, UNK 21992 50 MG PROLONGED-RELEASE TABLET
125564831 12556483 2 SS PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 100 MG, UNK 21992 100 MG PROLONGED-RELEASE TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125564831 12556483 1 Depression

Outcome of event

Event ID CASEID OUTC COD
125564831 12556483 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125564831 12556483 Activities of daily living impaired
125564831 12556483 Antisocial behaviour
125564831 12556483 Balance disorder
125564831 12556483 Disturbance in attention
125564831 12556483 Eye pain
125564831 12556483 Fall
125564831 12556483 Gait disturbance
125564831 12556483 Gastrointestinal disorder
125564831 12556483 Headache
125564831 12556483 Impaired driving ability
125564831 12556483 Nausea
125564831 12556483 Nervous system disorder
125564831 12556483 Paraesthesia
125564831 12556483 Vomiting
125564831 12556483 Withdrawal syndrome

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

no results found

Therapies reported

no results found