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
122835302 12283530 2 F 201507 20160927 20160419 20160930 PER US-JAZZ-2015-US-010800 JAZZ 25.14 YR M Y 81.63000 KG 20160930 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
122835302 12283530 1 PS XYREM SODIUM OXYBATE 1 Oral 2.25 G, BID 21196 2.25 G ORAL SOLUTION
122835302 12283530 2 C CLARITIN LORATADINE 1 UNK U 0 TABLET
122835302 12283530 3 C NUVIGIL ARMODAFINIL 1 UNK U 0 TABLET
122835302 12283530 4 C RITALIN METHYLPHENIDATE HYDROCHLORIDE 1 UNK U 0 TABLET
122835302 12283530 5 C TYLENOL ACETAMINOPHEN 1 UNK U 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122835302 12283530 1 Narcolepsy
122835302 12283530 2 Product used for unknown indication
122835302 12283530 3 Product used for unknown indication
122835302 12283530 4 Product used for unknown indication
122835302 12283530 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
122835302 12283530 Activities of daily living impaired
122835302 12283530 Drug dose omission
122835302 12283530 Intervertebral disc protrusion
122835302 12283530 Memory impairment
122835302 12283530 Pain
122835302 12283530 Somnolence

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
122835302 12283530 1 201507 20150813 0
122835302 12283530 2 20150601 0
122835302 12283530 3 20150601 0
122835302 12283530 4 20150601 0
122835302 12283530 5 20150601 0