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                Important Safety Information for Parsabiv®
              
              Contraindication: Parsabiv® (etelcalcetide) is
                contraindicated in patients with known hypersensitivity to etelcalcetide or any of its excipients.
                Hypersensitivity reactions, including face edema and anaphylactic reaction, have occurred.
              
              Hypocalcemia: Parsabiv® lowers serum calcium and can
                lead to hypocalcemia, sometimes severe. Significant lowering of serum calcium can cause QT interval
                prolongation and ventricular arrhythmia. Patients with conditions that predispose to QT interval
                prolongation and ventricular arrhythmia may be at increased risk for QT interval prolongation and
                ventricular arrhythmias if they develop hypocalcemia due to Parsabiv®. Closely monitor
                corrected serum calcium and QT interval in patients at risk on Parsabiv®.
              
              
                Significant reductions in corrected serum calcium may lower the threshold for seizures. Patients with a
                history of seizure disorder may be at increased risk for seizures if they develop hypocalcemia due to
                Parsabiv®. Monitor corrected serum calcium in patients with seizure disorders on
                Parsabiv®.
              
              
                Concurrent administration of Parsabiv® with another oral calcimimetic could result in
                severe, life-threatening hypocalcemia. Patients switching from cinacalcet to Parsabiv®
                should discontinue cinacalcet for at least 7 days prior to initiating Parsabiv®. Closely
                monitor corrected serum calcium in patients receiving Parsabiv® and concomitant therapies
                known to lower serum calcium.
              
              
                Measure corrected serum calcium prior to initiation of Parsabiv®. Do not initiate in
                patients if the corrected serum
                calcium is less than the lower limit of normal. Monitor corrected serum calcium within 1 week after
                initiation or dose
                adjustment and every 4 weeks during treatment with Parsabiv®. Measure PTH 4 weeks after
                initiation or dose adjustment of
                Parsabiv®. Once the maintenance dose has been established, measure PTH per clinical
                practice.
              
              Worsening Heart Failure: In Parsabiv
® clinical studies,
              cases of hypotension, congestive heart failure, and decreased myocardial performance have been reported.
              Closely monitor patients treated with Parsabiv
® for worsening signs and symptoms of heart
              failure.
              
              
                Upper Gastrointestinal Bleeding: In clinical studies, 2 patients
                treated with Parsabiv® in 1253 patient years of exposure had upper gastrointestinal (GI)
                bleeding at the time of death. The exact cause of GI bleeding in these patients is unknown and there
                were too few cases to determine whether these cases were related to Parsabiv®.
              
              
                Patients with risk factors for upper GI bleeding, such as known gastritis, esophagitis, ulcers or severe
                vomiting, may be at increased risk for GI bleeding with Parsabiv®. Monitor patients for
                worsening of common Parsabiv® GI adverse reactions and for signs and symptoms of GI
                bleeding and ulcerations during Parsabiv® therapy.
              
              
                Adynamic Bone: Adynamic bone may develop if PTH levels are chronically
                suppressed.
              
              
                Adverse Reactions: In clinical trials of patients with secondary HPT
                comparing Parsabiv® to placebo, the most common adverse reactions were blood calcium
                decreased (64% vs. 10%), muscle spasms (12% vs. 7%), diarrhea (11% vs. 9%), nausea (11% vs. 6%),
                vomiting (9% vs. 5%), headache (8% vs. 6%), hypocalcemia (7% vs. 0.2%), and paresthesia (6% vs. 1%).
              
              Indication
              
                Parsabiv® (etelcalcetide) is indicated for the treatment of secondary hyperparathyroidism
                (HPT) in adult patients with chronic kidney disease (CKD) on hemodialysis.
              
								Limitations of Use: Parsabiv® has not been studied in adult patients with parathyroid carcinoma, primary
									hyperparathyroidism, or with CKD who are not on hemodialysis and is not recommended for use in these
									populations.
							
							
								
									Limitations of Use:
									Parsabiv® has not been studied in adult patients with parathyroid carcinoma, primary
									hyperparathyroidism, or with CKD who are not on hemodialysis and is not recommended for use in these
									populations.
							 
								
              
                Please see Parsabiv® (etelcalcetide) full Prescribing
                  Information.