The Safety Rates Drug Report

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Drug     Injury     Quarter    

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