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
127244801 12724480 1 I 20160822 0 20160906 20160906 DIR US-FDA-349849 FDA-CTU 60.21 YR M N 74.25000 KG 20160906 N 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
127244801 12724480 1 PS HYDROCODONE BITARTRATE AND ACETAMINOPHEN ACETAMINOPHENHYDROCODONE BITARTRATE 1 Oral Y Y 20170818 0 180 DF COATED TABLET Q4H
127244801 12724480 3 C OXYGEN. OXYGEN 1 0
127244801 12724480 5 C COQ10 UBIDECARENONE 1 0
127244801 12724480 7 C SENIORS MEN MULTI VIT 2 0
127244801 12724480 9 C MELATONIN MELATONIN 1 0
127244801 12724480 11 C VITAMIN E .ALPHA.-TOCOPHEROL 1 0
127244801 12724480 13 C VITAMIN D CHOLECALCIFEROL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127244801 12724480 1 Intervertebral disc protrusion

Outcome of event

Event ID CASEID OUTC COD
127244801 12724480 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
127244801 12724480 Decreased appetite
127244801 12724480 Diarrhoea
127244801 12724480 Dizziness
127244801 12724480 Drug ineffective
127244801 12724480 Insomnia
127244801 12724480 Malaise
127244801 12724480 Seizure
127244801 12724480 Vomiting
127244801 12724480 Withdrawal syndrome

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

no results found

Therapies reported

no results found