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
127798351 12779835 1 I 0 20160925 20160925 DIR US-FDA-351456 FDA-CTU 20.00 YR F N 45.00000 KG 20160925 N 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
127798351 12779835 1 PS BUPROPION HCL SR 150MG SANDOZ BUPROPION HYDROCHLORIDE 1 Oral Y Y ME150125 20180330 99 30 DF COATED TABLET
127798351 12779835 2 SS LAMICTAL LAMOTRIGINE 1 Oral AT BEDTIME Y D 99 HS

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127798351 12779835 1 Depression
127798351 12779835 2 Depression

Outcome of event

Event ID CASEID OUTC COD
127798351 12779835 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
127798351 12779835 Anxiety
127798351 12779835 Arthralgia
127798351 12779835 Constipation
127798351 12779835 Decreased appetite
127798351 12779835 Eye irritation
127798351 12779835 Eye pain
127798351 12779835 Hyperhidrosis
127798351 12779835 Insomnia
127798351 12779835 Irritability
127798351 12779835 Mood altered
127798351 12779835 Myalgia
127798351 12779835 Oropharyngeal pain
127798351 12779835 Photosensitivity reaction
127798351 12779835 Rash
127798351 12779835 Skin exfoliation
127798351 12779835 Suicidal ideation
127798351 12779835 Tachycardia
127798351 12779835 Thirst
127798351 12779835 Weight decreased

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

Event ID CASEID RPSR COD
127798351 12779835 FGN

Therapies reported

no results found