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
126543311 12654331 1 I 20160812 0 20160815 20160815 DIR 47.00 YR F N 150.00000 LBS 20160813 N 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
126543311 12654331 1 PS VENLAFAXINE HCL VENLAFAXINE HYDROCHLORIDE 1 Oral 3 TABLET (S) IN THE MORNING TAKEN BY MOUTH 20170713 0 3 DF COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126543311 12654331 1 Depression

Outcome of event

Event ID CASEID OUTC COD
126543311 12654331 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126543311 12654331 Crying
126543311 12654331 Discomfort
126543311 12654331 Disorientation
126543311 12654331 Dissociation
126543311 12654331 Dizziness
126543311 12654331 Drug dose omission
126543311 12654331 Drug withdrawal syndrome
126543311 12654331 Feeling abnormal
126543311 12654331 Malaise
126543311 12654331 Pain
126543311 12654331 Paraesthesia
126543311 12654331 Photosensitivity reaction
126543311 12654331 Somnolence
126543311 12654331 Vomiting

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
126543311 12654331 1 20160713 20160811 0