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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125274671 | 12527467 | 1 | I | 20140812 | 20160622 | 20160705 | 20160705 | EXP | JP-PFIZER INC-2016314232 | PFIZER | 88.00 | YR | F | Y | 46.00000 | KG | 20160705 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125274671 | 12527467 | 1 | PS | HALCION | TRIAZOLAM | 1 | Oral | 0.125 MG, 1X/DAY | 394 | MG | Y | 17892 | .125 | MG | TABLET | QD | |||
125274671 | 12527467 | 2 | SS | HALCION | TRIAZOLAM | 1 | Oral | 0.125 MG, 1X/DAY | 394 | MG | Y | 17892 | .125 | MG | TABLET | QD | |||
125274671 | 12527467 | 3 | C | JZOLOFT | SERTRALINE HYDROCHLORIDE | 1 | Oral | 25 MG, 1X/DAY | 0 | 25 | MG | TABLET | QD | ||||||
125274671 | 12527467 | 4 | C | SANCOBA | CYANOCOBALAMIN | 1 | Ophthalmic | 0 | EYE DROPS, SOLUTION | ||||||||||
125274671 | 12527467 | 5 | C | HYALEIN | HYALURONATE SODIUM | 1 | Ophthalmic | 0 | EYE DROPS, SOLUTION | ||||||||||
125274671 | 12527467 | 6 | C | MOBIC | MELOXICAM | 1 | Oral | 10 MG, 1X/DAY | 0 | 10 | MG | TABLET | QD | ||||||
125274671 | 12527467 | 7 | C | RANITIDINE. | RANITIDINE | 1 | Oral | 75 MG, 2X/DAY | 0 | 75 | MG | BID |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125274671 | 12527467 | 1 | Insomnia |
125274671 | 12527467 | 3 | Depression |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125274671 | 12527467 | HO |
125274671 | 12527467 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125274671 | 12527467 | Abdominal discomfort | |
125274671 | 12527467 | Daydreaming | |
125274671 | 12527467 | Dementia | |
125274671 | 12527467 | Dizziness | |
125274671 | 12527467 | Gait disturbance | |
125274671 | 12527467 | Headache | |
125274671 | 12527467 | Hypoaesthesia | |
125274671 | 12527467 | Inappropriate schedule of drug administration | |
125274671 | 12527467 | Incontinence | |
125274671 | 12527467 | Insomnia | |
125274671 | 12527467 | Muscular weakness | |
125274671 | 12527467 | Nausea | |
125274671 | 12527467 | Reduced facial expression | |
125274671 | 12527467 | Somnolence | |
125274671 | 12527467 | 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 |
---|---|---|---|---|---|---|
125274671 | 12527467 | 1 | 20060117 | 0 | ||
125274671 | 12527467 | 2 | 20060117 | 20140902 | 0 |