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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126552541 | 12655254 | 1 | I | 201512 | 20160105 | 20160816 | 20160816 | PER | US-MYLANLABS-2016M1000953 | MYLAN | 0.00 | F | Y | 0.00000 | 20160816 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126552541 | 12655254 | 1 | PS | LITHIUM. | LITHIUM | 1 | Oral | 450 MG, QD | 202288 | 450 | MG | MODIFIED-RELEASE TABLET | QD | ||||||
| 126552541 | 12655254 | 2 | SS | LITHIUM. | LITHIUM | 1 | Oral | 300 MG, QD | 0 | 300 | MG | MODIFIED-RELEASE TABLET | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126552541 | 12655254 | 1 | Mania |
| 126552541 | 12655254 | 2 | Mania |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126552541 | 12655254 | Abdominal pain upper | |
| 126552541 | 12655254 | Dyspepsia | |
| 126552541 | 12655254 | Tremor |
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 |
|---|---|---|---|---|---|---|
| 126552541 | 12655254 | 1 | 201512 | 0 | ||
| 126552541 | 12655254 | 2 | 201512 | 0 |