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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126694511 | 12669451 | 1 | I | 201508 | 20160629 | 20160819 | 20160819 | PER | US-LUNDBECK-DKLU2015927 | LUNDBECK | 64.56 | YR | F | Y | 0.00000 | 20160819 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126694511 | 12669451 | 1 | PS | NORTHERA | DROXIDOPA | 1 | Unknown | U | 203202 | 100 | MG | TID | |||||||
| 126694511 | 12669451 | 2 | SS | NORTHERA | DROXIDOPA | 1 | Unknown | U | 203202 | 200 | MG | TID | |||||||
| 126694511 | 12669451 | 3 | SS | NORTHERA | DROXIDOPA | 1 | Unknown | U | 203202 | 300 | MG | TID | |||||||
| 126694511 | 12669451 | 4 | SS | MELOXICAM. | MELOXICAM | 1 | Unknown | Y | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126694511 | 12669451 | 1 | Product used for unknown indication |
| 126694511 | 12669451 | 4 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126694511 | 12669451 | Abdominal discomfort | |
| 126694511 | 12669451 | Arthralgia | |
| 126694511 | 12669451 | Back pain | |
| 126694511 | 12669451 | Occult blood positive | |
| 126694511 | 12669451 | Presyncope |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |