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
126905692 12690569 2 F 20160902 20160826 20160912 EXP US-JAZZ-2016-US-015756 JAZZ 0.00 F Y 0.00000 20160912 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
126905692 12690569 1 PS XYREM SODIUM OXYBATE 1 Oral 2.25 G, BID U 21196 2.25 G ORAL SOLUTION
126905692 12690569 2 SS XYREM SODIUM OXYBATE 1 2.5 G, BID U 21196 2.5 G ORAL SOLUTION
126905692 12690569 3 SS XYREM SODIUM OXYBATE 1 Oral 2.25 G, BID U 21196 2.25 G ORAL SOLUTION
126905692 12690569 4 SS XYREM SODIUM OXYBATE 1 Oral 2.25 G, BID U 21196 2.25 G ORAL SOLUTION
126905692 12690569 5 SS XYREM SODIUM OXYBATE 1 Oral 3 G, BID U 21196 3 G ORAL SOLUTION
126905692 12690569 6 SS WELLBUTRIN BUPROPION HYDROCHLORIDE 1 UNK 0 TABLET
126905692 12690569 7 C AMLODIPINE BESYLATE. AMLODIPINE BESYLATE 1 UNK U 0 TABLET
126905692 12690569 8 C ASPIRIN. ASPIRIN 1 UNK U 0 CHEWABLE TABLET
126905692 12690569 9 C ATENOLOL. ATENOLOL 1 UNK U 0 TABLET
126905692 12690569 10 C EFFIENT PRASUGREL HYDROCHLORIDE 1 UNK U 0 TABLET
126905692 12690569 11 C LIPITOR ATORVASTATIN CALCIUM 1 UNK U 0 TABLET
126905692 12690569 12 C NITROSTAT NITROGLYCERIN 1 UNK U 0 TABLET
126905692 12690569 13 C RANEXA RANOLAZINE 1 UNK U 0 TABLET
126905692 12690569 14 C FUROSEMIDE. FUROSEMIDE 1 UNK U 0 TABLET
126905692 12690569 15 C SINGULAIR MONTELUKAST SODIUM 1 UNK U 0 TABLET
126905692 12690569 16 C PRILOSEC OMEPRAZOLE MAGNESIUM 1 UNK U 0 CAPSULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126905692 12690569 1 Narcolepsy
126905692 12690569 2 Cataplexy
126905692 12690569 6 Product used for unknown indication
126905692 12690569 7 Product used for unknown indication
126905692 12690569 8 Product used for unknown indication
126905692 12690569 9 Product used for unknown indication
126905692 12690569 10 Product used for unknown indication
126905692 12690569 11 Product used for unknown indication
126905692 12690569 12 Product used for unknown indication
126905692 12690569 13 Product used for unknown indication
126905692 12690569 14 Product used for unknown indication
126905692 12690569 15 Product used for unknown indication
126905692 12690569 16 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126905692 12690569 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126905692 12690569 Coronary artery disease
126905692 12690569 Drug hypersensitivity
126905692 12690569 Feeling abnormal

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
126905692 12690569 1 200211 200808 0
126905692 12690569 2 200808 200908 0
126905692 12690569 3 200908 2009 0
126905692 12690569 4 201109 201109 0
126905692 12690569 5 201109 201509 0
126905692 12690569 6 201608 0
126905692 12690569 7 201608 0
126905692 12690569 8 201608 0
126905692 12690569 9 201608 0
126905692 12690569 10 201608 0
126905692 12690569 11 201608 0
126905692 12690569 12 201608 0
126905692 12690569 13 201608 0
126905692 12690569 14 20121221 201608 0
126905692 12690569 15 20121221 0
126905692 12690569 16 201312 0