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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127208241 | 12720824 | 1 | I | 20160902 | 20160907 | 20160907 | EXP | CA-SCIEGEN PHARMACEUTICALS INC-2016SCILIT00404 | SCIEGEN | 39.00 | YR | M | Y | 0.00000 | 20160907 | MD | CA | CA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127208241 | 12720824 | 1 | PS | BUPROPION HYDROCHLORIDE EXTENDED-RELEASE TABLETS USP, 150 MG | BUPROPION HYDROCHLORIDE | 1 | Unknown | UNK | U | 206122 | TABLET | ||||||||
| 127208241 | 12720824 | 2 | SS | ESCITALOPRAM | ESCITALOPRAM OXALATE | 1 | Unknown | UNK | U | 0 | |||||||||
| 127208241 | 12720824 | 3 | SS | OLANZAPINE. | OLANZAPINE | 1 | Unknown | UNK | U | 0 | |||||||||
| 127208241 | 12720824 | 4 | SS | PHENYTOIN. | PHENYTOIN | 1 | Unknown | UNK | U | 0 | |||||||||
| 127208241 | 12720824 | 5 | SS | PRIMIDONE. | PRIMIDONE | 1 | Unknown | UNK | U | 0 | |||||||||
| 127208241 | 12720824 | 6 | SS | QUETAPINE | QUETIAPINE | 1 | Unknown | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127208241 | 12720824 | 1 | Product used for unknown indication |
| 127208241 | 12720824 | 2 | Product used for unknown indication |
| 127208241 | 12720824 | 3 | Product used for unknown indication |
| 127208241 | 12720824 | 4 | Product used for unknown indication |
| 127208241 | 12720824 | 5 | Product used for unknown indication |
| 127208241 | 12720824 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127208241 | 12720824 | HO |
| 127208241 | 12720824 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127208241 | 12720824 | Agitation | |
| 127208241 | 12720824 | Arrhythmia | |
| 127208241 | 12720824 | Confusional state | |
| 127208241 | 12720824 | Delirium | |
| 127208241 | 12720824 | Device related sepsis | |
| 127208241 | 12720824 | Hyperhidrosis | |
| 127208241 | 12720824 | Hyperreflexia | |
| 127208241 | 12720824 | Hyperthermia | |
| 127208241 | 12720824 | Incoherent | |
| 127208241 | 12720824 | Major depression | |
| 127208241 | 12720824 | Muscle rigidity | |
| 127208241 | 12720824 | Myoclonus | |
| 127208241 | 12720824 | Neuroleptic malignant syndrome | |
| 127208241 | 12720824 | Overdose | |
| 127208241 | 12720824 | Pneumonia | |
| 127208241 | 12720824 | Seizure | |
| 127208241 | 12720824 | Serotonin syndrome | |
| 127208241 | 12720824 | Tachycardia | |
| 127208241 | 12720824 | Tremor |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |