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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7117346 | 7679203 | I | 7117346-9 | 20101116 | 20101122 | EXP | DE-CEPHALON-2010006035 | CEPHALON | YR | M | Y | 20101122 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7117346 | 1015167205 | PS | FENTANYL CITRATE | 1 | 021947 | ||||||
| 7117346 | 1015167206 | C | MORPHINE | 1 | |||||||
| 7117346 | 1015167207 | C | CISPLATIN | 1 | |||||||
| 7117346 | 1015167208 | C | DICLOFENAC SODIUM | 1 | |||||||
| 7117346 | 1015167209 | C | AMITRIPTYLINE HCL | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7117346 | 1015167206 | BREAKTHROUGH PAIN |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 7117346 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 7117346 | CONSTIPATION |
| 7117346 | DECREASED APPETITE |
| 7117346 | DISTURBANCE IN ATTENTION |
| 7117346 | DIZZINESS |
| 7117346 | DRUG PRESCRIBING ERROR |
| 7117346 | FATIGUE |
| 7117346 | GENERAL PHYSICAL HEALTH DETERIORATION |
| 7117346 | HYPERHIDROSIS |
| 7117346 | NAUSEA |
| 7117346 | SLEEP DISORDER |
| 7117346 | UNEVALUABLE EVENT |
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 |
|---|---|---|---|---|---|
| 7117346 | 1015167205 | 20100412 |