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
125380701 12538070 1 I 20160627 20160707 20160707 EXP US-009507513-1606USA013413 MERCK 0.00 F Y 0.00000 20160707 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
125380701 12538070 1 PS REMERON MIRTAZAPINE 1 Oral 7.5 MG, UNK U 20415 7.5 MG TABLET
125380701 12538070 2 SS PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 Oral UNK U 0 TABLET
125380701 12538070 3 SS PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 Oral UNK U 0 TABLET

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
125380701 12538070 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125380701 12538070 Adverse event
125380701 12538070 Anxiety
125380701 12538070 Drug intolerance
125380701 12538070 Feeding disorder
125380701 12538070 Feeling abnormal
125380701 12538070 Nausea
125380701 12538070 Night sweats
125380701 12538070 Somnolence
125380701 12538070 Weight decreased

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
125380701 12538070 3 20150920 0