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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126271862 | 12627186 | 2 | F | 20160630 | 20160909 | 20160805 | 20160921 | EXP | FR-AFSSAPS-PA20160637 | FR-FRI-1000086671 | FOREST | 22.87 | YR | F | Y | 0.00000 | 20160921 | OT | DK | FR |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126271862 | 12627186 | 1 | PS | ESCITALOPRAM | ESCITALOPRAM OXALATE | 1 | Oral | 10 MG | Y | 21323 | 10 | MG | QD | ||||||
126271862 | 12627186 | 2 | SS | ESCITALOPRAM | ESCITALOPRAM OXALATE | 1 | Oral | OVERDOSE: ESCITALOPRAM 280 MG AT ONCE. | Y | 21323 | 280 | MG | |||||||
126271862 | 12627186 | 3 | SS | DOXYLAMINE | DOXYLAMINE | 1 | Oral | Y | 0 | ||||||||||
126271862 | 12627186 | 4 | SS | NOCERTONE | OXETORONE | 1 | Oral | Y | 0 | 1.2 | G | ||||||||
126271862 | 12627186 | 5 | SS | CODEINE | CODEINE | 1 | Oral | Y | 0 | 120 | MG | ||||||||
126271862 | 12627186 | 6 | C | PARACETAMOL | ACETAMINOPHEN | 1 | Oral | 0 | 2 | G | |||||||||
126271862 | 12627186 | 7 | C | KETOPROFENE | KETOPROFEN | 1 | Oral | 0 | 700 | MG | |||||||||
126271862 | 12627186 | 8 | C | KETOPROFENE | KETOPROFEN | 1 | Oral | OVERDOSE: KETOPROFENE 700 MG AT ONCE. | 0 | 700 | MG | ||||||||
126271862 | 12627186 | 9 | C | JASMINELLE | DROSPIRENONE | 1 | Unknown | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126271862 | 12627186 | 1 | Depression |
126271862 | 12627186 | 3 | Product used for unknown indication |
126271862 | 12627186 | 4 | Product used for unknown indication |
126271862 | 12627186 | 5 | Product used for unknown indication |
126271862 | 12627186 | 6 | Product used for unknown indication |
126271862 | 12627186 | 7 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126271862 | 12627186 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126271862 | 12627186 | Dry mouth | |
126271862 | 12627186 | Miosis | |
126271862 | 12627186 | Somnolence |
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 |
---|---|---|---|---|---|---|
126271862 | 12627186 | 1 | 20160630 | 0 | ||
126271862 | 12627186 | 2 | 20160630 | 20160630 | 0 | |
126271862 | 12627186 | 3 | 20160630 | 0 | ||
126271862 | 12627186 | 4 | 20160630 | 20160630 | 0 | |
126271862 | 12627186 | 5 | 20160630 | 20160630 | 0 | |
126271862 | 12627186 | 6 | 20160630 | 20160630 | 0 | |
126271862 | 12627186 | 7 | 20160630 | 0 | ||
126271862 | 12627186 | 8 | 20160630 | 20160630 | 0 |