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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
108684735 | 10868473 | 5 | F | 201511 | 20160823 | 20150225 | 20160831 | EXP | US-LUNDBECK-DKLU1108444 | LUNDBECK | 45.11 | YR | F | Y | 0.00000 | 20160831 | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
108684735 | 10868473 | 1 | PS | NORTHERA | DROXIDOPA | 1 | Unknown | VSNH | 203202 | 100 | MG | TID | |||||||
108684735 | 10868473 | 2 | SS | NORTHERA | DROXIDOPA | 1 | Unknown | VSNH | 203202 | 300 | MG | TID | |||||||
108684735 | 10868473 | 3 | SS | NORTHERA | DROXIDOPA | 1 | Unknown | VSNH | 203202 | 600 | MG | ||||||||
108684735 | 10868473 | 4 | SS | NORTHERA | DROXIDOPA | 1 | Unknown | TITRATED TO 600 MG | VSNH | 203202 | |||||||||
108684735 | 10868473 | 5 | SS | NORTHERA | DROXIDOPA | 1 | Unknown | TAPERED DOWN TO 300 MG | VSNH | 203202 | |||||||||
108684735 | 10868473 | 6 | SS | PREDNISONE. | PREDNISONE | 1 | Unknown | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
108684735 | 10868473 | 1 | Autonomic neuropathy |
108684735 | 10868473 | 2 | Syncope |
108684735 | 10868473 | 6 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
108684735 | 10868473 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
108684735 | 10868473 | Blood pressure increased | |
108684735 | 10868473 | Candida infection | |
108684735 | 10868473 | Chest pain | |
108684735 | 10868473 | Dizziness | |
108684735 | 10868473 | Drug effect decreased | |
108684735 | 10868473 | Feeling abnormal | |
108684735 | 10868473 | Headache | |
108684735 | 10868473 | Heart rate increased | |
108684735 | 10868473 | Respiratory failure |
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 |
---|---|---|---|---|---|---|
108684735 | 10868473 | 1 | 20150129 | 0 | ||
108684735 | 10868473 | 3 | 201511 | 0 | ||
108684735 | 10868473 | 4 | 201607 | 0 | ||
108684735 | 10868473 | 6 | 201506 | 0 |