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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4747898 | 5865842 | I | 4747898-5 | 20050603 | 20050817 | DIR | 62 | YR | F | N | 215 | LBS | 20050816 | OT | 20050604 | N | Y | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4747898 | 1006332127 | PS | FENTANYL | 1 | TRANSDERMAL | 50MG EVERY 72 HOURS TRANSDERMAL | D | D |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4747898 | 1006332127 | PAIN |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4747898 | DE |
Reactions reported
| Event ID | PT |
|---|---|
| 4747898 | ABDOMINAL DISTENSION |
| 4747898 | ACCIDENTAL OVERDOSE |
| 4747898 | ANOXIC ENCEPHALOPATHY |
| 4747898 | ASTHENIA |
| 4747898 | BLOOD PRESSURE IMMEASURABLE |
| 4747898 | CARDIAC ARREST |
| 4747898 | CONVULSION |
| 4747898 | DIAPHRAGMATIC RUPTURE |
| 4747898 | HYPOVENTILATION |
| 4747898 | IATROGENIC INJURY |
| 4747898 | INTESTINAL INFARCTION |
| 4747898 | LETHARGY |
| 4747898 | MALAISE |
| 4747898 | POST PROCEDURAL NAUSEA |
| 4747898 | RENAL FAILURE |
| 4747898 | RESPIRATORY RATE DECREASED |
| 4747898 | SEPTIC SHOCK |
| 4747898 | SPEECH DISORDER |
| 4747898 | TREMOR |
| 4747898 | WHITE BLOOD CELL COUNT DECREASED |
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 |
|---|---|---|---|---|---|
| 4747898 | 1006332127 | 20050526 | 20050604 |