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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7790310 | 8164362 | I | 7790310-2 | 20110919 | 20110930 | EXP | DE-MYLANLABS-2011S1019490 | MYLAN PHARMACEUTICALS INC. | 70 | YR | F | Y | 20110930 | CN | GERMANY |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7790310 | 1017681496 | C | IRBESARTAN | 1 | ORAL | ||||||
| 7790310 | 1017681495 | PS | GABAPENTIN | 1 | ORAL | 090335 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7790310 | 1017681496 | HYPERTENSION |
| 7790310 | 1017681495 | PAIN IN EXTREMITY |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 7790310 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 7790310 | ABDOMINAL PAIN UPPER |
| 7790310 | SOMNOLENCE |
| 7790310 | PRURITUS |
| 7790310 | ANXIETY |
| 7790310 | DYSPNOEA |
| 7790310 | MUSCLE SPASMS |
| 7790310 | NERVOUSNESS |
| 7790310 | PYREXIA |
| 7790310 | MYALGIA |
| 7790310 | DECREASED APPETITE |
| 7790310 | NAUSEA |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 7790310 | 1017681495 | 20110401 | 20110912 |