The Safety Rates Drug Report

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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
127089431 12708943 1 I 2016 20160504 20160901 20160901 PER US-JAZZ-2016-US-008415 JAZZ 0.00 F Y 0.00000 20160901 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
127089431 12708943 1 PS XYREM SODIUM OXYBATE 1 Oral 2.25 G, BID 21196 2.25 G ORAL SOLUTION
127089431 12708943 2 SS ADDERALL AMPHETAMINE ASPARTATEAMPHETAMINE SULFATEDEXTROAMPHETAMINE SACCHARATEDEXTROAMPHETAMINE SULFATE 1 UNK Y 0
127089431 12708943 3 SS NUVIGIL ARMODAFINIL 1 UNK Y 0
127089431 12708943 4 SS RITALIN METHYLPHENIDATE HYDROCHLORIDE 1 UNK Y 0
127089431 12708943 5 C LISINOPRIL. LISINOPRIL 1 U 0
127089431 12708943 6 C AMOXICILLIN. AMOXICILLIN 1 U 0
127089431 12708943 7 C ASPIRIN. ASPIRIN 1 U 0
127089431 12708943 8 C PAXIL PAROXETINE HYDROCHLORIDE 1 U 0
127089431 12708943 9 C KLONOPIN CLONAZEPAM 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127089431 12708943 1 Narcolepsy
127089431 12708943 2 Product used for unknown indication
127089431 12708943 3 Product used for unknown indication
127089431 12708943 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127089431 12708943 Abnormal dreams
127089431 12708943 Condition aggravated
127089431 12708943 Dizziness
127089431 12708943 Drug ineffective

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
127089431 12708943 1 201604 0
127089431 12708943 2 2016 0
127089431 12708943 3 2016 0
127089431 12708943 4 2016 0