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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 114171842 | 11417184 | 2 | F | 201411 | 20150623 | 20150825 | 20160726 | PER | US-MYLANLABS-2015M1021245 | MYLAN | 78.71 | YR | F | Y | 43.84000 | KG | 20160726 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 114171842 | 11417184 | 1 | PS | PAROXETINE HYDROCHLORIDE. | PAROXETINE HYDROCHLORIDE | 1 | Oral | 12.5 MG, QD | 77873 | 12.5 | MG | MODIFIED-RELEASE TABLET | QD | ||||||
| 114171842 | 11417184 | 2 | SS | PAROXETINE HYDROCHLORIDE. | PAROXETINE HYDROCHLORIDE | 1 | 77873 | MODIFIED-RELEASE TABLET | |||||||||||
| 114171842 | 11417184 | 3 | SS | PAROXETINE HYDROCHLORIDE. | PAROXETINE HYDROCHLORIDE | 1 | 77873 | MODIFIED-RELEASE TABLET | |||||||||||
| 114171842 | 11417184 | 4 | SS | Nicardipine Hydrochloride Capsules | NICARDIPINE HYDROCHLORIDE | 1 | Oral | 20 MG, QID | Y | 0 | 20 | MG | CAPSULE | QID | |||||
| 114171842 | 11417184 | 5 | SS | Nicardipine Hydrochloride Capsules | NICARDIPINE HYDROCHLORIDE | 1 | Oral | 20 MG, TID | Y | 0 | 20 | MG | CAPSULE | TID | |||||
| 114171842 | 11417184 | 6 | C | AMBIEN | ZOLPIDEM TARTRATE | 1 | UNK | 0 | |||||||||||
| 114171842 | 11417184 | 7 | C | XANAX | ALPRAZOLAM | 1 | UNK | 0 | |||||||||||
| 114171842 | 11417184 | 8 | C | CLONIDINE. | CLONIDINE | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 114171842 | 11417184 | 1 | Blood pressure increased |
| 114171842 | 11417184 | 2 | Cardiac flutter |
| 114171842 | 11417184 | 3 | Off label use |
| 114171842 | 11417184 | 8 | Hypertension |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 114171842 | 11417184 | Blood pressure increased | |
| 114171842 | 11417184 | Burning sensation | |
| 114171842 | 11417184 | Drug interaction | |
| 114171842 | 11417184 | Hypersensitivity | |
| 114171842 | 11417184 | Palpitations | |
| 114171842 | 11417184 | Rash pruritic | |
| 114171842 | 11417184 | Tremor | |
| 114171842 | 11417184 | Weight decreased |
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 |
|---|---|---|---|---|---|---|
| 114171842 | 11417184 | 1 | 201411 | 0 | ||
| 114171842 | 11417184 | 4 | 201411 | 0 |