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
128001901 12800190 1 I 20160915 20160930 20160930 EXP GB-B. BRAUN MEDICAL INC.-1057892 B BRAUN 55.00 YR M Y 0.00000 20160930 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
128001901 12800190 1 PS LIDOCAINE HYDROCHLORIDE AND DEXTROSE DEXTROSELIDOCAINE HYDROCHLORIDE 1 Parenteral 19830 30 MG
128001901 12800190 2 SS CHIROCAINE LEVOBUPIVACAINE HYDROCHLORIDE 1 Parenteral 0 .5 PCT
128001901 12800190 3 SS FENTANYL. FENTANYL 1 Parenteral 0 100 UG
128001901 12800190 4 SS MIDAZOLAM MIDAZOLAMMIDAZOLAM HYDROCHLORIDE 1 Parenteral 0 5 MG
128001901 12800190 5 SS SODIUM CHLORIDE. SODIUM CHLORIDE 1 0
128001901 12800190 6 SS triamcinolone TRIAMCINOLONE 1 Parenteral 0 86 MG
128001901 12800190 7 C CLONAZEPAM. CLONAZEPAM 1 0 2 MG
128001901 12800190 8 C EPILIM VALPROATE SODIUM 1 0 100 MG
128001901 12800190 9 C GABAPENTIN. GABAPENTIN 1 0 400 MG
128001901 12800190 10 C Glucosamine Sulphate GLUCOSAMINE 1 0 750 MG
128001901 12800190 11 C MORPHINE SULFATE. MORPHINE SULFATE 1 0
128001901 12800190 12 C RANITIDINE. RANITIDINE 1 0 150 MG
128001901 12800190 13 C TRAMADOL. TRAMADOL 1 0 50 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
128001901 12800190 1 Facet joint block

Outcome of event

Event ID CASEID OUTC COD
128001901 12800190 HO
128001901 12800190 DS
128001901 12800190 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
128001901 12800190 Ageusia
128001901 12800190 Amnesia
128001901 12800190 Circulatory collapse
128001901 12800190 Decreased appetite
128001901 12800190 Discomfort
128001901 12800190 Dissociative amnesia
128001901 12800190 Dysgeusia
128001901 12800190 Dysgraphia
128001901 12800190 Erythema
128001901 12800190 Eye pain
128001901 12800190 Facial paralysis
128001901 12800190 Hallucination
128001901 12800190 Headache
128001901 12800190 Hemiparesis
128001901 12800190 Hypoaesthesia oral
128001901 12800190 Loss of consciousness
128001901 12800190 Muscle spasms
128001901 12800190 Muscle twitching
128001901 12800190 Muscular weakness
128001901 12800190 Musculoskeletal stiffness
128001901 12800190 Mydriasis
128001901 12800190 Nausea
128001901 12800190 Nightmare
128001901 12800190 Ocular hyperaemia
128001901 12800190 Pain
128001901 12800190 Photosensitivity reaction
128001901 12800190 Rash
128001901 12800190 Skin warm
128001901 12800190 Speech disorder
128001901 12800190 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
128001901 12800190 1 20140904 20140904 0
128001901 12800190 2 20140904 20140904 0
128001901 12800190 3 20140904 20140904 0
128001901 12800190 4 20140904 20140904 0
128001901 12800190 5 20140904 20140904 0
128001901 12800190 6 20140904 20140904 0