The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
6026597 6879837 I 6026597-6 20081001 20081217 20081231 EXP 038473 BARR LABORATORIES 53 YR F N 52.2 KG 20081230 UNITED STATES

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
6026597 1010947347 PS ADDERALL 10 1 D D 11522
6026597 1010964016 SS BUSPAR 1 D D
6026597 1010964017 SS CELEBREX 1 200 MG, 2 IN 1 D, U U
6026597 1010964018 SS CHANTIX 1 0.5 MG, 1 IN 1 D, D D
6026597 1010964019 SS EFFEXOR 1 75 MG, 1 IN 1 D, U U
6026597 1010964020 SS VALIUM 1 5 MG, 2 IN 1 D, D D
6026597 1010964022 C DEPAKOTE 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
6026597 1010947347 ATTENTION DEFICIT/HYPERACTIVITY DISORDER
6026597 1010964017 ARTHRITIS
6026597 1010964018 SMOKING CESSATION THERAPY
6026597 1010964019 DEPRESSION

Outcome of event

Event ID OUTC COD
6026597 OT

Reactions reported

Event ID PT
6026597 AGITATION
6026597 CHEST DISCOMFORT
6026597 CONDITION AGGRAVATED
6026597 DEPRESSION
6026597 DYSPNOEA
6026597 ECONOMIC PROBLEM
6026597 FEELING ABNORMAL
6026597 NAUSEA
6026597 SUICIDAL IDEATION

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

Event ID RPSR COD
6026597 CSM
6026597 OTH

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6026597 1010964017 20081001 20081101
6026597 1010964018 20081101