The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
5958971 7025965 I 5958971-8 20081031 20081117 EXP 2008ST000242 SANTARUS, INC. 78 YR F N 20081112 MD UNITED KINGDOM

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
5958971 1010725499 PS ZEGERID 1 Y D 21636
5958971 1010746659 C SPIRONOLACTONE 1 21636
5958971 1010746660 C BUMETANIDE 1 21636
5958971 1010746661 C FUROSEMIDE 2 21636
5958971 1010746662 C GABAPENTIN 1 21636
5958971 1010746663 C ACETAMINOPHEN W/ CODEINE 1 21636
5958971 1010746670 C HYOSCINE HBR HYT 1 21636
5958971 1010746671 C GLYCERYL TRINITRATE 2 21636
5958971 1010746672 C LOSARTAN POTASSIUM 1 21636
5958971 1010746674 C ASPIRIN 1 21636
5958971 1010746676 C ATORVASTATIN CALCIUM 1 21636
5958971 1010746679 C IPRATROPIUM BROMIDE 1 21636
5958971 1010746680 SS SALMETEROL 2 21636

Indications of drugs used

Event ID DRUG SEQ INDI PT
5958971 1010725499 DIVERTICULUM
5958971 1010725499 DUODENITIS
5958971 1010725499 HIATUS HERNIA

Outcome of event

Event ID OUTC COD
5958971 HO
5958971 OT
5958971 RI

Reactions reported

Event ID PT
5958971 CHRONIC OBSTRUCTIVE PULMONARY DISEASE
5958971 HYPOCALCAEMIA
5958971 HYPOKALAEMIA
5958971 HYPOMAGNESAEMIA
5958971 HYPOPHOSPHATAEMIA
5958971 NO THERAPEUTIC RESPONSE
5958971 OEDEMA PERIPHERAL

Reporting Sources (this data is often not reported and may therefore be missing here)

Event ID RPSR COD
5958971 FGN
5958971 HP
5958971 LIT

Therapies reported

no results found