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
125240081 12524008 1 I 2015 20151221 20160704 20160704 PER US-JAZZ-2015-US-022169 JAZZ 73.63 YR M Y 73.92000 KG 20160704 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
125240081 12524008 1 PS XYREM SODIUM OXYBATE 1 Oral 2.25 G, BID 21196 2.25 G ORAL SOLUTION
125240081 12524008 2 SS XYREM SODIUM OXYBATE 1 Oral 3 G, BID 21196 3 G ORAL SOLUTION
125240081 12524008 3 C MIRAPEX PRAMIPEXOLE DIHYDROCHLORIDE 1 UNK U 0 TABLET
125240081 12524008 4 C LIPITOR ATORVASTATIN CALCIUM 1 UNK U 0
125240081 12524008 5 C PRILOSEC OMEPRAZOLE MAGNESIUM 1 UNK U 0
125240081 12524008 6 C Baby aspirin ASPIRIN 1 UNK U 0
125240081 12524008 7 C FLUTICASONE FLUTICASONEFLUTICASONE PROPIONATE 1 UNK U 0 NASAL SPRAY
125240081 12524008 8 C Aspirin adult 2 UNK U 0 CHEWABLE TABLET
125240081 12524008 9 C Atorvastatin ATORVASTATIN 1 UNK U 0 TABLET
125240081 12524008 10 C COMBIVENT ALBUTEROL SULFATEIPRATROPIUM BROMIDE 1 UNK U 0 INHALER
125240081 12524008 11 C Flonase allergy rlf 2 UNK U 0 SPRAY
125240081 12524008 12 C Multivitamin VITAMINS 1 UNK U 0 TABLET
125240081 12524008 13 C NAPROXEN SODIUM. NAPROXEN SODIUM 1 UNK U 0
125240081 12524008 14 C OMEPRAZOLE DR OMEPRAZOLE 1 UNK U 0 CAPSULE
125240081 12524008 15 C Potassium gluconate POTASSIUM GLUCONATE 1 UNK U 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125240081 12524008 1 Narcolepsy
125240081 12524008 3 Restless legs syndrome
125240081 12524008 4 Blood cholesterol increased
125240081 12524008 5 Prophylaxis
125240081 12524008 6 Product used for unknown indication
125240081 12524008 7 Rhinorrhoea
125240081 12524008 8 Product used for unknown indication
125240081 12524008 9 Product used for unknown indication
125240081 12524008 10 Product used for unknown indication
125240081 12524008 11 Product used for unknown indication
125240081 12524008 12 Product used for unknown indication
125240081 12524008 13 Product used for unknown indication
125240081 12524008 14 Product used for unknown indication
125240081 12524008 15 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125240081 12524008 Condition aggravated
125240081 12524008 Fall
125240081 12524008 Feeling abnormal
125240081 12524008 Gait disturbance
125240081 12524008 Injury
125240081 12524008 Loss of consciousness
125240081 12524008 Oropharyngeal pain
125240081 12524008 Somnambulism
125240081 12524008 Unevaluable event

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
125240081 12524008 1 20151207 201512 0
125240081 12524008 2 201512 0
125240081 12524008 3 20151119 0
125240081 12524008 8 20151119 0
125240081 12524008 9 20151119 0
125240081 12524008 10 20151119 0
125240081 12524008 11 20151119 0
125240081 12524008 12 20151119 0
125240081 12524008 13 20151119 0
125240081 12524008 14 20151119 0
125240081 12524008 15 20151119 0