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
126413261 12641326 1 I 20160802 20160810 20160810 PER US-PFIZER INC-2016372697 PFIZER 0.00 M Y 0.00000 20160810 MD 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
126413261 12641326 1 PS PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 Oral 100 MG, 1X/DAY Y 21992 100 MG PROLONGED-RELEASE TABLET QD
126413261 12641326 2 SS PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 Oral 50 MG, 1X/DAY Y 21992 50 MG PROLONGED-RELEASE TABLET QD
126413261 12641326 3 SS EFFEXOR VENLAFAXINE HYDROCHLORIDE 1 150 MG, UNK U 20699 150 MG TABLET
126413261 12641326 4 C ATORVASTATIN ATORVASTATIN 1 80 MG, UNK 0 80 MG
126413261 12641326 5 C OXYCODONE OXYCODONE 1 40 MG, UNK 0 40 MG
126413261 12641326 6 C CLONAZEPAM. CLONAZEPAM 1 1 MG, AS NEEDED 0 1 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126413261 12641326 1 Depression

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126413261 12641326 Anxiety
126413261 12641326 Decreased appetite
126413261 12641326 Disturbance in attention
126413261 12641326 Irritability
126413261 12641326 Nightmare
126413261 12641326 Norepinephrine decreased
126413261 12641326 Paraesthesia
126413261 12641326 Poor quality sleep
126413261 12641326 Serum serotonin increased

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126413261 12641326 2 20160421 0
126413261 12641326 3 2016 0