Person who experienced the adverse event (patient)
| Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5327084 | 6314191 | I | 5327084-0 | 20070508 | 20070517 | EXP | PHEH2007US07035 | NOVARTIS PHARMACEUTICALS CORP. | F | Y | 20070517 | UNITED STATES |
Drug(s) used by person
| Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5327084 | 1008487301 | PS | ZELNORM | 1 | ORAL | 6 MG, BID | 021200 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5327084 | 1008487301 | IRRITABLE BOWEL SYNDROME |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5327084 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5327084 | ANXIETY |
| 5327084 | DISTURBANCE IN ATTENTION |
| 5327084 | DIZZINESS |
| 5327084 | DRUG WITHDRAWAL SYNDROME |
| 5327084 | FEELING ABNORMAL |
| 5327084 | HEADACHE |
| 5327084 | HEART RATE INCREASED |
| 5327084 | HYPOGLYCAEMIA |
| 5327084 | INSOMNIA |
| 5327084 | PANIC ATTACK |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |