The Safety Rates Drug Report

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Drug     Injury     Quarter    

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
127706831 12770683 1 I 20140905 20160913 20160922 20160922 EXP GB-JNJFOC-20160914854 JANSSEN 55.00 YR A M Y 0.00000 20160922 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
127706831 12770683 1 PS FENTANYL. FENTANYL 1 Transdermal N U 19813 100 DF MATRIX PATCH
127706831 12770683 2 SS TRIAMCINOLONE TRIAMCINOLONE 1 Unknown N 0 86 DF UNSPECIFIED
127706831 12770683 3 SS NORMAL SALINE SODIUM CHLORIDE 1 Unknown N 0 UNSPECIFIED
127706831 12770683 4 SS MIDAZOLAM MIDAZOLAMMIDAZOLAM HYDROCHLORIDE 1 Unknown N 0 5 DF UNSPECIFIED
127706831 12770683 5 SS LIDOCAINE. LIDOCAINE 1 Unknown N 0 30 DF UNSPECIFIED
127706831 12770683 6 SS LEVOBUPIVACAINE HYDROCHLORIDE LEVOBUPIVACAINE HYDROCHLORIDE 1 Unknown N 0 13 DF UNSPECIFIED
127706831 12770683 7 C TRAMADOL. TRAMADOL 1 Unknown 1 OR 2 D 0 UNSPECIFIED
127706831 12770683 8 C MORPHINE SULFATE. MORPHINE SULFATE 1 Unknown 10 MG /5 ML D 0 UNSPECIFIED
127706831 12770683 9 C GLUCOSAMINE SULPHATE GLUCOSAMINE 1 Unknown D 0 2 DF UNSPECIFIED QD
127706831 12770683 10 C GABAPENTIN. GABAPENTIN 1 Unknown D 0 400 DF UNSPECIFIED
127706831 12770683 11 C EPILIM VALPROATE SODIUM 1 Unknown D 0 100 DF UNSPECIFIED QD
127706831 12770683 12 C CLONAZEPAM. CLONAZEPAM 1 Unknown D 0 2 DF UNSPECIFIED BID
127706831 12770683 13 C RANITIDINE. RANITIDINE 1 Unknown 1 TO 2 DAILY D 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127706831 12770683 1 Sedation
127706831 12770683 2 Sedation
127706831 12770683 3 Sedation
127706831 12770683 4 Sedation
127706831 12770683 5 Sedation
127706831 12770683 6 Sedation
127706831 12770683 8 Breakthrough pain

Outcome of event

Event ID CASEID OUTC COD
127706831 12770683 HO
127706831 12770683 OT
127706831 12770683 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
127706831 12770683 Ageusia
127706831 12770683 Amnesia
127706831 12770683 Circulatory collapse
127706831 12770683 Decreased appetite
127706831 12770683 Discomfort
127706831 12770683 Dissociative amnesia
127706831 12770683 Dysgeusia
127706831 12770683 Dysgraphia
127706831 12770683 Erythema
127706831 12770683 Eye pain
127706831 12770683 Facial paralysis
127706831 12770683 Hallucination
127706831 12770683 Headache
127706831 12770683 Hemiparesis
127706831 12770683 Hypoaesthesia oral
127706831 12770683 Loss of consciousness
127706831 12770683 Muscle spasms
127706831 12770683 Muscle twitching
127706831 12770683 Muscular weakness
127706831 12770683 Musculoskeletal stiffness
127706831 12770683 Mydriasis
127706831 12770683 Nausea
127706831 12770683 Nightmare
127706831 12770683 Ocular hyperaemia
127706831 12770683 Pain
127706831 12770683 Photosensitivity reaction
127706831 12770683 Rash pruritic
127706831 12770683 Skin warm
127706831 12770683 Speech disorder
127706831 12770683 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
127706831 12770683 1 20140904 20140904 0
127706831 12770683 2 20140904 20140904 0
127706831 12770683 3 20140904 20140904 0
127706831 12770683 4 20140904 20140904 0
127706831 12770683 5 20140904 20140904 0
127706831 12770683 6 20140904 20140904 0