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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125582101 | 12558210 | 1 | I | 2012 | 20160708 | 20160714 | 20160714 | EXP | PHEH2016US017068 | NOVARTIS | 0.00 | M | Y | 81.65000 | KG | 20160714 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125582101 | 12558210 | 1 | PS | TEGRETOL | CARBAMAZEPINE | 1 | Oral | 200 MG, TID | 16608 | 200 | MG | TID | |||||||
| 125582101 | 12558210 | 2 | SS | LAMICTAL | LAMOTRIGINE | 1 | Oral | 2.5 DF, QD (HALF IN MORNING, ONE IN AFTERNOON AND ONE IN EVENING) | 0 | 2.5 | DF | QD | |||||||
| 125582101 | 12558210 | 3 | SS | LYRICA | PREGABALIN | 1 | Oral | 75 MG, BID (IN MORNING AND EVENING) | 0 | 75 | MG | BID | |||||||
| 125582101 | 12558210 | 4 | SS | KEPPRA | LEVETIRACETAM | 1 | Unknown | 250 MG, QD (IN EVENING) | N | 0 | 250 | MG | QD | ||||||
| 125582101 | 12558210 | 5 | SS | AVODART | DUTASTERIDE | 1 | Unknown | 0.5 MG, QD (IN EVENING) | 0 | .5 | MG | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125582101 | 12558210 | 1 | Epilepsy |
| 125582101 | 12558210 | 2 | Epilepsy |
| 125582101 | 12558210 | 3 | Seizure |
| 125582101 | 12558210 | 4 | Epilepsy |
| 125582101 | 12558210 | 5 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125582101 | 12558210 | OT |
| 125582101 | 12558210 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125582101 | 12558210 | Amnesia | |
| 125582101 | 12558210 | Blood pressure decreased | |
| 125582101 | 12558210 | Fall | |
| 125582101 | 12558210 | Hip fracture | |
| 125582101 | 12558210 | Loss of consciousness |
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 |
|---|---|---|---|---|---|---|
| 125582101 | 12558210 | 5 | 2014 | 0 |