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
124719022 12471902 2 F 20160604 20160810 20160616 20160817 EXP JP-PFIZER INC-2016299800 PFIZER 27.00 YR F Y 0.00000 20160817 PH JP JP

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
124719022 12471902 1 PS EFFEXOR VENLAFAXINE HYDROCHLORIDE 1 Oral 75 MG, 1X/DAY 750 MG 20699 75 MG PROLONGED-RELEASE CAPSULE QD
124719022 12471902 2 SS SEDIEL TANDOSPIRONE 1 Oral 2 DF, 2X/DAY 40 DF 0 2 DF TABLET BID
124719022 12471902 3 SS BELSOMRA SUVOREXANT 1 Oral UNK 0
124719022 12471902 4 SS LUNESTA ESZOPICLONE 1 Oral 2 MG, 1X/DAY 20 MG 0 2 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124719022 12471902 1 Depression
124719022 12471902 2 Depression
124719022 12471902 3 Insomnia
124719022 12471902 4 Insomnia

Outcome of event

Event ID CASEID OUTC COD
124719022 12471902 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124719022 12471902 Altered state of consciousness

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
124719022 12471902 1 20160526 20160604 0
124719022 12471902 2 20160526 20160604 0
124719022 12471902 3 20160526 20160604 0
124719022 12471902 4 20160526 20160604 0