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
125564341 12556434 1 I 20151223 20160617 20160714 20160714 EXP US-AMGEN-USASL2016079674 AMGEN 65.00 YR E F Y 62.13000 KG 20160714 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
125564341 12556434 1 PS PROLIA DENOSUMAB 1 Subcutaneous 60 MG/ML, Q6MO 125320 SOLUTION FOR INJECTION
125564341 12556434 2 C VITAMIN B12 CYANOCOBALAMIN 1 1 MG, QMO 0 1 MG /month
125564341 12556434 3 C VOLTAREN DICLOFENAC SODIUM 1 UNK UNK, AS NECESSARY 0
125564341 12556434 4 C LIDOCAINE. LIDOCAINE 1 Topical UNK UNK, AS NECESSARY 0
125564341 12556434 5 C LORAZEPAM. LORAZEPAM 1 1 MG, Q6H 0 1 MG QID
125564341 12556434 6 C ASPIRIN. ASPIRIN 1 81 MG, QD 0 81 MG QD
125564341 12556434 7 C COREG CARVEDILOL 1 25 MG, BID 0 25 MG BID
125564341 12556434 8 C GABAPENTIN. GABAPENTIN 1 300 MG, TID 0 300 MG TID
125564341 12556434 9 C LISINOPRIL. LISINOPRIL 1 10 MG, BID 0 10 MG BID
125564341 12556434 10 C MAGNESIUM OXIDE. MAGNESIUM OXIDE 1 250 MG, BID 0 250 MG BID
125564341 12556434 11 C OXYBUTYNIN OXYBUTYNIN 1 5 MG, QD 0 5 MG QD
125564341 12556434 12 C SPIRONOLACTONE. SPIRONOLACTONE 1 25 MG, QD 0 25 MG QD
125564341 12556434 13 C TIZANIDINE. TIZANIDINE 1 4 MG, QD 0 4 MG QD
125564341 12556434 14 C EFFEXOR VENLAFAXINE HYDROCHLORIDE 1 75 MG, BID 0 75 MG BID
125564341 12556434 15 C VITAMIN D CHOLECALCIFEROL 1 0
125564341 12556434 16 C CALCIUM CALCIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125564341 12556434 1 Osteoporosis postmenopausal
125564341 12556434 5 Anxiety

Outcome of event

Event ID CASEID OUTC COD
125564341 12556434 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125564341 12556434 Adverse reaction
125564341 12556434 Bone pain
125564341 12556434 Cystitis
125564341 12556434 Drug intolerance
125564341 12556434 Dysuria
125564341 12556434 Hypersensitivity
125564341 12556434 Injection site pruritus
125564341 12556434 Pelvic fracture
125564341 12556434 Pruritus
125564341 12556434 Skin fissures
125564341 12556434 Urticaria

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
125564341 12556434 1 20151223 0