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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127245361 | 12724536 | 1 | I | 20160825 | 20160908 | 20160908 | EXP | NP-MLMSERVICE-20160819-0398181-1 | NP-ALKEM LABORATORIES LIMITED-NP-ALKEM-2016-00164 | ALKEM | 23.00 | YR | F | Y | 0.00000 | 20160908 | CN | GB | NP |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127245361 | 12724536 | 1 | PS | AMLODIPINE BESYLATE. | AMLODIPINE BESYLATE | 1 | Oral | 220 MG, AT ONCE | 78925 | 220 | MG | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127245361 | 12724536 | 1 | Suicidal ideation |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127245361 | 12724536 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127245361 | 12724536 | Dizziness | |
| 127245361 | 12724536 | Hypotension | |
| 127245361 | 12724536 | Intentional overdose | |
| 127245361 | 12724536 | Myocardial depression | |
| 127245361 | 12724536 | Overdose | |
| 127245361 | 12724536 | Pulmonary oedema | |
| 127245361 | 12724536 | Respiratory alkalosis | |
| 127245361 | 12724536 | Suicide attempt | |
| 127245361 | 12724536 | Swelling face |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |