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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126619381 | 12661938 | 1 | I | 20160815 | 20160817 | 20160817 | PER | PHEH2016US020588 | NOVARTIS | 0.00 | M | Y | 0.00000 | 20160817 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126619381 | 12661938 | 1 | PS | EXELON PATCH | RIVASTIGMINE | 1 | Transdermal | 4.6 MG, QD (PATCH 5 (CM2), 09 MG DAILY?RIVASTIGMINE BASE) | U | 4405C | 22083 | 4.6 | MG | TRANS-THERAPEUTIC-SYSTEM | QD | ||||
| 126619381 | 12661938 | 2 | C | BUPROPION. | BUPROPION | 1 | Unknown | UNK | U | 0 | |||||||||
| 126619381 | 12661938 | 3 | C | PRAVASTATIN. | PRAVASTATIN | 1 | Unknown | UNK | U | 0 | |||||||||
| 126619381 | 12661938 | 4 | C | LISINOPRIL. | LISINOPRIL | 1 | Unknown | UNK | U | 0 | |||||||||
| 126619381 | 12661938 | 5 | C | MULTI VITAMIN | VITAMINS | 1 | Unknown | UNK | U | 0 | |||||||||
| 126619381 | 12661938 | 6 | C | ASPIRIN. | ASPIRIN | 1 | Unknown | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126619381 | 12661938 | 1 | Product used for unknown indication |
| 126619381 | 12661938 | 2 | Product used for unknown indication |
| 126619381 | 12661938 | 3 | Product used for unknown indication |
| 126619381 | 12661938 | 4 | Product used for unknown indication |
| 126619381 | 12661938 | 5 | Product used for unknown indication |
| 126619381 | 12661938 | 6 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126619381 | 12661938 | Hyperhidrosis | |
| 126619381 | 12661938 | Product adhesion issue |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |