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
101209273 10120927 3 F 20100216 20160920 20140425 20160929 EXP PHHO2010US03791 NOVARTIS 78.96 YR F Y 68.00000 KG 20160929 MD 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
101209273 10120927 1 PS RECLAST ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 5 MG, YEARLY Y U 21817 5 MG
101209273 10120927 2 C CELECOXIB. CELECOXIB 1 Unknown UNK 0
101209273 10120927 3 C CELECOXIB. CELECOXIB 1 UNK 0
101209273 10120927 4 C NAPROXEN. NAPROXEN 1 Unknown UNK 0
101209273 10120927 5 C NAPROXEN. NAPROXEN 1 UNK 0
101209273 10120927 6 C IBUPROFEN. IBUPROFEN 1 Unknown UNK 0
101209273 10120927 7 C IBUPROFEN. IBUPROFEN 1 Unknown UNK 0
101209273 10120927 8 C NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral UNK 0
101209273 10120927 9 C NEXIUM ESOMEPRAZOLE MAGNESIUM 1 UNK 0
101209273 10120927 10 C METHOTREXATE. METHOTREXATE 1 Oral UNK 0
101209273 10120927 11 C PREDNISONE. PREDNISONE 1 Oral UNK 0
101209273 10120927 12 C FOLIC ACID. FOLIC ACID 1 Oral UNK 0
101209273 10120927 13 C SIMVASTATIN. SIMVASTATIN 1 Oral UNK 0
101209273 10120927 14 C MULTIVITAMINS, PLAIN VITAMINS 1 Oral UNK 0
101209273 10120927 15 C CALCIUM CALCIUM 1 Oral UNK 0
101209273 10120927 16 C VITAMIN D CHOLECALCIFEROL 1 Oral UNK 0
101209273 10120927 17 C DOXEPIN DOXEPIN 1 Oral UNK 0
101209273 10120927 18 C METAMUCIL PLANTAGO SEED 1 Oral UNK U 0
101209273 10120927 19 C ALTACE RAMIPRIL 1 Oral UNK 0
101209273 10120927 20 C NORVASC AMLODIPINE BESYLATE 1 Oral UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
101209273 10120927 1 Osteoporosis
101209273 10120927 2 Rheumatoid arthritis
101209273 10120927 4 Rheumatoid arthritis
101209273 10120927 6 Rheumatoid arthritis
101209273 10120927 8 Prophylaxis
101209273 10120927 10 Product used for unknown indication
101209273 10120927 11 Product used for unknown indication
101209273 10120927 12 Product used for unknown indication
101209273 10120927 13 Product used for unknown indication
101209273 10120927 14 Product used for unknown indication
101209273 10120927 15 Product used for unknown indication
101209273 10120927 16 Product used for unknown indication
101209273 10120927 17 Product used for unknown indication
101209273 10120927 18 Product used for unknown indication
101209273 10120927 19 Product used for unknown indication
101209273 10120927 20 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
101209273 10120927 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
101209273 10120927 Abdominal pain upper
101209273 10120927 Hypokalaemia
101209273 10120927 Hyponatraemia
101209273 10120927 Nausea
101209273 10120927 Vomiting

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
101209273 10120927 1 20100215 20100215 0
101209273 10120927 2 20090219 20100223 0
101209273 10120927 3 20100225 0
101209273 10120927 4 20090219 20100223 0
101209273 10120927 5 20100225 0
101209273 10120927 6 20090220 20100223 0
101209273 10120927 7 20100225 20121003 0
101209273 10120927 8 20090220 20100223 0
101209273 10120927 9 20100225 0
101209273 10120927 10 20000821 0
101209273 10120927 11 20000508 0
101209273 10120927 12 20000821 0
101209273 10120927 13 19980318 0
101209273 10120927 14 20000821 0
101209273 10120927 15 20000821 0
101209273 10120927 16 20000821 0
101209273 10120927 17 20000821 0
101209273 10120927 18 20070403 0
101209273 10120927 19 19981209 0
101209273 10120927 20 20090930 0