Person who experienced the adverse event (patient)
Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127901771 | 12790177 | 1 | I | 20160915 | 20160913 | 20160928 | 20160928 | EXP | GB-MHRA-EYC 00145023 | GB-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-075488 | BRISTOL MYERS SQUIBB | 55.00 | YR | M | Y | 0.00000 | 20160928 | CN | GB | GB |
Drug(s) used by person
Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127901771 | 12790177 | 1 | PS | TRIAMCINOLONE ACETONIDE. | TRIAMCINOLONE ACETONIDE | 1 | Parenteral | D | SQUIBB | 12041 | 86 | MG | INJECTION | ||||||
127901771 | 12790177 | 2 | SS | CHIROCAINE | LEVOBUPIVACAINE HYDROCHLORIDE | 1 | Parenteral | 13 ML, UNK | D | ABBOTT | 0 | 13 | ML | ||||||
127901771 | 12790177 | 3 | SS | FENTANYL. | FENTANYL | 1 | Parenteral | 100 DF, UNK | D | U | HAMELN PHARMACEUTICALS | 0 | 100 | DF | |||||
127901771 | 12790177 | 4 | SS | LIDOCAINE. | LIDOCAINE | 1 | Parenteral | 30 MG, UNK | D | U | B BRAUN | 0 | 30 | MG | |||||
127901771 | 12790177 | 5 | SS | MIDAZOLAM | MIDAZOLAMMIDAZOLAM HYDROCHLORIDE | 1 | Parenteral | 5 MG, UNK | D | U | MERCURY PHARMA | 0 | 5 | MG | |||||
127901771 | 12790177 | 6 | SS | NORMAL SALINE | SODIUM CHLORIDE | 1 | Parenteral | UNK | U | U | FENNING | 0 | |||||||
127901771 | 12790177 | 7 | C | CLONAZEPAM. | CLONAZEPAM | 1 | Unknown | U | 0 | 2 | MG | BID | |||||||
127901771 | 12790177 | 8 | C | EPILIM | VALPROATE SODIUM | 1 | Unknown | U | 0 | 100 | MG | QD | |||||||
127901771 | 12790177 | 9 | C | GABAPENTIN. | GABAPENTIN | 1 | Unknown | PLUS EXTRA DOSE AT NIGHT. | U | 0 | 400 | MG | |||||||
127901771 | 12790177 | 10 | C | GLUCOSAMINE SULPHATE | GLUCOSAMINE | 1 | Unknown | U | 0 | 2 | DF | QD | |||||||
127901771 | 12790177 | 11 | C | MORPHINE SULFATE. | MORPHINE SULFATE | 1 | Unknown | 10MG/5ML | U | 0 | |||||||||
127901771 | 12790177 | 12 | C | RANITIDINE. | RANITIDINE | 1 | Unknown | 1-2 ONCE DAILY | U | 0 | |||||||||
127901771 | 12790177 | 13 | C | TRAMADOL. | TRAMADOL | 1 | Unknown | ONE OR TWO 4 TIMES DAILY. | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127901771 | 12790177 | 1 | Sedation |
127901771 | 12790177 | 2 | Sedation |
127901771 | 12790177 | 3 | Sedation |
127901771 | 12790177 | 4 | Sedation |
127901771 | 12790177 | 5 | Sedation |
127901771 | 12790177 | 6 | Sedation |
127901771 | 12790177 | 7 | Product used for unknown indication |
127901771 | 12790177 | 8 | Product used for unknown indication |
127901771 | 12790177 | 9 | Product used for unknown indication |
127901771 | 12790177 | 10 | Product used for unknown indication |
127901771 | 12790177 | 11 | Breakthrough pain |
127901771 | 12790177 | 12 | Product used for unknown indication |
127901771 | 12790177 | 13 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127901771 | 12790177 | DS |
127901771 | 12790177 | OT |
127901771 | 12790177 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127901771 | 12790177 | Ageusia | |
127901771 | 12790177 | Amnesia | |
127901771 | 12790177 | Circulatory collapse | |
127901771 | 12790177 | Decreased appetite | |
127901771 | 12790177 | Discomfort | |
127901771 | 12790177 | Dissociative amnesia | |
127901771 | 12790177 | Dysgeusia | |
127901771 | 12790177 | Dysgraphia | |
127901771 | 12790177 | Erythema | |
127901771 | 12790177 | Eye pain | |
127901771 | 12790177 | Facial paralysis | |
127901771 | 12790177 | Hallucination | |
127901771 | 12790177 | Headache | |
127901771 | 12790177 | Hemiparesis | |
127901771 | 12790177 | Hypoaesthesia oral | |
127901771 | 12790177 | Loss of consciousness | |
127901771 | 12790177 | Muscle spasms | |
127901771 | 12790177 | Muscle twitching | |
127901771 | 12790177 | Muscular weakness | |
127901771 | 12790177 | Musculoskeletal stiffness | |
127901771 | 12790177 | Mydriasis | |
127901771 | 12790177 | Nausea | |
127901771 | 12790177 | Nightmare | |
127901771 | 12790177 | Ocular hyperaemia | |
127901771 | 12790177 | Pain | |
127901771 | 12790177 | Photosensitivity reaction | |
127901771 | 12790177 | Product use issue | |
127901771 | 12790177 | Rash | |
127901771 | 12790177 | Skin warm | |
127901771 | 12790177 | Speech disorder | |
127901771 | 12790177 | Unresponsive to stimuli |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|---|
127901771 | 12790177 | 1 | 20140904 | 20140904 | 0 | |
127901771 | 12790177 | 2 | 20140904 | 20140904 | 0 | |
127901771 | 12790177 | 3 | 20140904 | 20140904 | 0 | |
127901771 | 12790177 | 4 | 20140904 | 20140904 | 0 | |
127901771 | 12790177 | 5 | 20140904 | 20140904 | 0 | |
127901771 | 12790177 | 6 | 20140904 | 20140904 | 0 |