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
124914672 12491467 2 F 20160719 20160623 20160721 PER PHEH2016US015116 NOVARTIS 0.00 Y 0.00000 20160721 CN US US

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
124914672 12491467 1 PS TRILEPTAL OXCARBAZEPINE 1 Unknown UNK U 21014
124914672 12491467 2 SS VALIUM DIAZEPAM 1 Unknown UNK U 0
124914672 12491467 3 SS IMITREX SUMATRIPTAN SUCCINATE 1 Unknown UNK U 0
124914672 12491467 4 SS DEMEROL MEPERIDINE HYDROCHLORIDE 1 Unknown UNK U 0
124914672 12491467 5 SS CODEINE CODEINE 1 Unknown UNK U 0
124914672 12491467 6 SS MORPHINE MORPHINE 1 Unknown UNK U 0
124914672 12491467 7 SS TALWIN PENTAZOCINE LACTATE 1 Unknown UNK U 0
124914672 12491467 8 SS ACTONEL RISEDRONATE SODIUM 1 Unknown UNK U 0
124914672 12491467 9 SS FLEXERIL CYCLOBENZAPRINE HYDROCHLORIDE 1 Unknown UNK U 0
124914672 12491467 10 SS INDERAL PROPRANOLOL HYDROCHLORIDE 1 Unknown UNK U 0
124914672 12491467 11 SS NEURONTIN GABAPENTIN 1 Unknown UNK U 0
124914672 12491467 12 SS ULTRAM TRAMADOL HYDROCHLORIDE 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124914672 12491467 1 Product used for unknown indication
124914672 12491467 2 Product used for unknown indication
124914672 12491467 3 Product used for unknown indication
124914672 12491467 4 Product used for unknown indication
124914672 12491467 5 Product used for unknown indication
124914672 12491467 6 Product used for unknown indication
124914672 12491467 7 Product used for unknown indication
124914672 12491467 8 Product used for unknown indication
124914672 12491467 9 Product used for unknown indication
124914672 12491467 10 Product used for unknown indication
124914672 12491467 11 Product used for unknown indication
124914672 12491467 12 Seizure

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124914672 12491467 Hypersensitivity

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found