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
126508271 12650827 1 I 2013 20160314 20160815 20160815 PER US-JAZZ-2016-US-004927 JAZZ 0.00 F Y 0.00000 20160815 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
126508271 12650827 1 PS XYREM SODIUM OXYBATE 1 Oral 1.5 G, BID U 21196 1.5 G ORAL SOLUTION
126508271 12650827 2 SS XYREM SODIUM OXYBATE 1 Oral 3 G, BID U 21196 3 G ORAL SOLUTION
126508271 12650827 3 SS XYREM SODIUM OXYBATE 1 Oral 4.5 G, BID U 21196 4.5 G ORAL SOLUTION
126508271 12650827 4 SS NUVIGIL ARMODAFINIL 1 UNK U 0 TABLET
126508271 12650827 5 C LINZESS LINACLOTIDE 1 U 0
126508271 12650827 6 C Centrum VITAMINS 1 U 0
126508271 12650827 7 C NUVARING ETHINYL ESTRADIOLETONOGESTREL 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126508271 12650827 1 Narcolepsy
126508271 12650827 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126508271 12650827 Headache

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
126508271 12650827 1 201307 201308 0
126508271 12650827 2 201308 201309 0
126508271 12650827 3 201309 0
126508271 12650827 4 20050701 0