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
126916182 12691618 2 F 20160902 20160826 20160912 EXP US-BAUSCH-BL-2016-020693 BAUSCH AND LOMB 0.00 F Y 0.00000 20160912 CN 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
126916182 12691618 1 SS XYREM SODIUM OXYBATE 1 Oral U 0 2.25 G ORAL SOLUTION BID
126916182 12691618 2 SS XYREM SODIUM OXYBATE 1 Oral U 0 2.5 G ORAL SOLUTION BID
126916182 12691618 3 SS XYREM SODIUM OXYBATE 1 Oral U 0 2.25 G ORAL SOLUTION BID
126916182 12691618 4 SS XYREM SODIUM OXYBATE 1 Oral U 0 2.25 G ORAL SOLUTION BID
126916182 12691618 5 SS XYREM SODIUM OXYBATE 1 Oral U 0 3 G ORAL SOLUTION BID
126916182 12691618 6 PS WELLBUTRIN BUPROPION HYDROCHLORIDE 1 Unknown 21515 TABLET
126916182 12691618 7 C AMLODIPINE BESYLATE. AMLODIPINE BESYLATE 1 0 TABLET
126916182 12691618 8 C ASPIRIN. ASPIRIN 1 0 CHEWABLE TABLET
126916182 12691618 9 C ATENOLOL. ATENOLOL 1 0 TABLET
126916182 12691618 10 C EFFIENT PRASUGREL HYDROCHLORIDE 1 0 TABLET
126916182 12691618 11 C LIPITOR ATORVASTATIN CALCIUM 1 0 TABLET
126916182 12691618 12 C NITROSTAT NITROGLYCERIN 1 0 TABLET
126916182 12691618 13 C RANEXA RANOLAZINE 1 0 TABLET
126916182 12691618 14 C FUROSEMIDE. FUROSEMIDE 1 0 TABLET
126916182 12691618 15 C SINGULAIR MONTELUKAST SODIUM 1 0 TABLET
126916182 12691618 16 C PRILOSEC OMEPRAZOLE MAGNESIUM 1 0 CAPSULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126916182 12691618 1 Narcolepsy
126916182 12691618 2 Cataplexy
126916182 12691618 6 Product used for unknown indication
126916182 12691618 7 Product used for unknown indication
126916182 12691618 8 Product used for unknown indication
126916182 12691618 9 Product used for unknown indication
126916182 12691618 10 Product used for unknown indication
126916182 12691618 11 Product used for unknown indication
126916182 12691618 12 Product used for unknown indication
126916182 12691618 13 Product used for unknown indication
126916182 12691618 14 Product used for unknown indication
126916182 12691618 15 Product used for unknown indication
126916182 12691618 16 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126916182 12691618 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126916182 12691618 Coronary artery disease
126916182 12691618 Drug hypersensitivity
126916182 12691618 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
126916182 12691618 1 200211 200808 0
126916182 12691618 2 200808 200908 0
126916182 12691618 3 200908 2009 0
126916182 12691618 4 201109 201109 0
126916182 12691618 5 201109 201509 0
126916182 12691618 6 201608 0
126916182 12691618 7 201608 0
126916182 12691618 8 201608 0
126916182 12691618 9 201608 0
126916182 12691618 10 201608 0
126916182 12691618 11 201608 0
126916182 12691618 12 201608 0
126916182 12691618 13 201608 0
126916182 12691618 14 20121221 201608 0
126916182 12691618 15 20121221 0
126916182 12691618 16 201312 0