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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127022321 | 12702232 | 1 | I | 20160817 | 20160831 | 20160831 | EXP | FR-NORTHSTAR HEALTHCARE HOLDINGS-FR-2016NSR001838 | NORTHSTAR | JAVELOT H, MICHEL B, MARQUIS A, DIDELOT N, SOCHA M, JAVELOT T, ET AL.. ACUTE WITHDRAWAL SYNDROME AFTER DISCONTINUATION OF A SHORT ANALGESIC TREATMENT WITH TRAMADOL. THERAPIE. 2016;71 (3):347-348 | 89.00 | YR | F | Y | 46.00000 | KG | 20160831 | OT | FR | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127022321 | 12702232 | 1 | PS | TRAMADOL HYDROCHLORIDE. | TRAMADOL HYDROCHLORIDE | 1 | Oral | UNK | Y | 78935 | |||||||||
| 127022321 | 12702232 | 2 | C | CHLORHEXIDINE | CHLORHEXIDINE | 1 | Topical | UNK | U | 0 | SPRAY (EXCEPT INHALATION) | ||||||||
| 127022321 | 12702232 | 3 | C | MEMANTINE. | MEMANTINE | 1 | 10 MG, QD | U | 0 | 10 | MG | ||||||||
| 127022321 | 12702232 | 4 | C | HYDROXYZINE | HYDROXYZINEHYDROXYZINE HYDROCHLORIDE | 1 | 25 MG, QD | U | 0 | 25 | MG | ||||||||
| 127022321 | 12702232 | 5 | C | LACTULOSE. | LACTULOSE | 1 | 10 G/15ML, BID | U | 0 | ||||||||||
| 127022321 | 12702232 | 6 | C | PAROXETINE. | PAROXETINE | 1 | 10 MG, QD | U | 0 | 10 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127022321 | 12702232 | 1 | Pain in extremity |
| 127022321 | 12702232 | 2 | Furuncle |
| 127022321 | 12702232 | 3 | Dementia Alzheimer's type |
| 127022321 | 12702232 | 4 | Product used for unknown indication |
| 127022321 | 12702232 | 5 | Product used for unknown indication |
| 127022321 | 12702232 | 6 | Depression |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127022321 | 12702232 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127022321 | 12702232 | Abdominal discomfort | |
| 127022321 | 12702232 | Clonus | |
| 127022321 | 12702232 | Disorientation | |
| 127022321 | 12702232 | Drug withdrawal syndrome | |
| 127022321 | 12702232 | Pain | |
| 127022321 | 12702232 | Vomiting |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |