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
127050791 12705079 1 I 20160826 0 20160831 20160831 DIR 33.00 YR F N 175.00000 LBS 20160829 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
127050791 12705079 1 PS ESCITALOPRAM ESCITALOPRAM OXALATE 1 Oral 1 TABLET(S) ONCE A DAY TAKEN BY MOUTH Y D 0 1 DF COATED TABLET QD
127050791 12705079 3 C MAGNESIUM MAGNESIUM 1 0
127050791 12705079 5 C PROBIOTIC PROBIOTICS NOS 1 0
127050791 12705079 7 C MULTI VITAMIN VITAMINS 1 0
127050791 12705079 9 C COENZYME Q 10 2 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127050791 12705079 1 Generalised anxiety disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127050791 12705079 Asthenia
127050791 12705079 Chills
127050791 12705079 Dizziness
127050791 12705079 Nausea
127050791 12705079 Presyncope

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
127050791 12705079 1 20160820 20160826 0