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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125682421 | 12568242 | 1 | I | 20151012 | 20160718 | 20160718 | PER | US-JUBILANT CADISTA PHARMACEUTICALS-2015JUB00328 | JUBILANT | 81.00 | YR | F | Y | 44.90000 | KG | 20160718 | CN | COUNTRY NOT SPECIFIED | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125682421 | 12568242 | 1 | PS | MECLIZINE HYDROCHLORIDE. | MECLIZINE HYDROCHLORIDE | 1 | UNK | U | 40659 | TABLET | |||||||||
| 125682421 | 12568242 | 2 | C | AMLODIPINE | AMLODIPINE BESYLATE | 1 | 2.5 MG, 1X/DAY | 0 | 2.5 | MG | QD | ||||||||
| 125682421 | 12568242 | 3 | C | AMLODIPINE | AMLODIPINE BESYLATE | 1 | 5 MG, UNK | 0 | 5 | MG | QD | ||||||||
| 125682421 | 12568242 | 4 | C | METOPROLOL. | METOPROLOL | 1 | 75 MG, 2X/DAY | 0 | 75 | MG | BID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125682421 | 12568242 | 1 | Vertigo |
| 125682421 | 12568242 | 4 | Blood pressure abnormal |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125682421 | 12568242 | Malaise | |
| 125682421 | 12568242 | Nausea | |
| 125682421 | 12568242 | Off label use |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |