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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5040244 | 6075328 | I | 5040244-1 | 20060620 | 20060630 | EXP | GB-JNJFOC-20060604124 | JOHNSON + JOHNSON PHARMACEUTICAL R+D | M | Y | 20060630 | CN | UNITED KINGDOM |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5040244 | 1007430368 | SS | DURAGESIC-50 | 1 | TRANSDERMAL | ||||||
5040244 | 1007430369 | SS | DURAGESIC-50 | 1 | TRANSDERMAL | ||||||
5040244 | 1007430370 | PS | DURAGESIC-50 | 1 | TRANSDERMAL | 019813 | |||||
5040244 | 1007430371 | SS | BUPRENORPHINE HCL | 1 | UNKNOWN | ||||||
5040244 | 1007430372 | SS | BUPRENORPHINE HCL | 1 | TRANSDERMAL |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5040244 | 1007430370 | BONE PAIN |
5040244 | 1007430371 | ANALGESIC EFFECT |
Outcome of event
Event ID | OUTC COD |
---|---|
5040244 | OT |
Reactions reported
Event ID | PT |
---|---|
5040244 | ANXIETY |
5040244 | APHASIA |
5040244 | ARRHYTHMIA |
5040244 | DEPRESSED MOOD |
5040244 | INCORRECT ROUTE OF DRUG ADMINISTRATION |
5040244 | RESPIRATORY DISORDER |
5040244 | SCREAMING |
5040244 | TREMOR |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |