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
106760722 10676072 2 F 20140111 20160923 20141225 20160927 EXP PHHY2014NL166676 SANDOZ 46.00 YR F Y 0.00000 20160927 CN US NL

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
106760722 10676072 1 SS BACLOFEN. BACLOFEN 1 Oral 10 MG, TID U 0 10 MG TID
106760722 10676072 2 SS BACLOFEN. BACLOFEN 1 Oral 700 MG, UNK (70 TABLETS OF 10 MG) U 0 700 MG
106760722 10676072 3 PS CLOMIPRAMINE CLOMIPRAMINE 1 Unknown 75 MG, QD U 74364 75 MG QD
106760722 10676072 4 SS OXAZEPAM. OXAZEPAM 1 Unknown 10 MG, QD U 0 10 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
106760722 10676072 1 Alcoholism
106760722 10676072 3 Product used for unknown indication
106760722 10676072 4 Alcoholism

Outcome of event

Event ID CASEID OUTC COD
106760722 10676072 LT
106760722 10676072 OT
106760722 10676072 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
106760722 10676072 Depressed level of consciousness
106760722 10676072 Disturbance in attention
106760722 10676072 Hallucination, auditory
106760722 10676072 Hyperhidrosis
106760722 10676072 Hypertension
106760722 10676072 Hypokalaemia
106760722 10676072 Hyponatraemia
106760722 10676072 Hypothermia
106760722 10676072 Intentional overdose
106760722 10676072 Mydriasis
106760722 10676072 Nausea
106760722 10676072 Respiratory failure
106760722 10676072 Restlessness
106760722 10676072 Toxicity to various agents
106760722 10676072 Vomiting

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

no results found

Therapies reported

no results found