Patient Assistance Programs - Amitiza

PATIENT ASSISTANCE PROGRAMS

AMITIZA PATIENT ASSISTANCE PROGRAM

The AMITIZA Patient Assistance Program gives patients who would otherwise find it financially difficult to receive treatment access to up to a year of free AMITIZA therapy.*

*Patients must meet Eligibility Requirements.

AMITIZA HEALTHY SAVINGS PROGRAM

The AMITIZA Healthy Savings Program allows your patients to receive up to $35 a month on AMITIZA prescriptions.*

*Patients must meet Eligibility Requirements.

TOGETHER RX ACCESS PROGRAM

Together Rx Access is a prescription savings program that offers a free, easy way to save on prescription medications.*

*Patients must meet Eligibility Requirements.

PARTNERSHIP FOR PRESCRIPTION ASSISTANCE

Partnership for Prescription Assistance is a single point of access to more than 475 public and private patient assistance programs.*

*Patients must meet Eligibility Requirements.

LEARN ABOUT THE AMITIZA PATIENT ASSISTANCE PROGRAM

Indication

AMITIZA (lubiprostone) is indicated for the treatment of Chronic Idiopathic Constipation (24 mcg twice daily) in adults and for Irritable Bowel Syndrome with Constipation (8 mcg twice daily) in women ≥ 18 years old.

Important Safety Information

AMITIZA is contraindicated in patients with known or suspected mechanical gastrointestinal obstruction. Patients with symptoms suggestive of mechanical gastrointestinal obstruction should be thoroughly evaluated by the treating healthcare provider to confirm the absence of such an obstruction prior to initiating AMITIZA treatment.
The safety of AMITIZA in pregnancy has not been evaluated in humans. AMITIZA should be used during pregnancy only if the benefit justifies the potential risk to the fetus. Women who could become pregnant should have a negative pregnancy test prior to beginning therapy with AMITIZA and should be capable of complying with effective contraceptive measures.
Patients taking AMITIZA may experience nausea. If this occurs, concomitant administration of food with AMITIZA may reduce symptoms of nausea. Patients who experience severe nausea should inform their healthcare provider.
AMITIZA should not be prescribed to patients that have severe diarrhea. Patients should be aware of the possible occurrence of diarrhea during treatment and inform their healthcare provider if the diarrhea becomes severe.
Patients taking AMITIZA may experience dyspnea within an hour of first dose. This symptom generally resolves within three hours, but may recur with repeat dosing. Patients who experience dyspnea should inform their healthcare provider. Some patients have discontinued therapy because of dyspnea.
In clinical trials of AMITIZA (24 mcg twice daily vs placebo; N=1113 vs N=316) in patients with Chronic Idiopathic Constipation (CIC), the most common adverse reactions (incidence > 4%) were nausea (29% vs 3%), diarrhea (12% vs < 1%), headache (11% vs 5%), abdominal pain (8% vs 3%), abdominal distension (6% vs 2%), and flatulence (6% vs 2%).
In clinical trials of AMITIZA (8 mcg twice daily vs placebo; N=1011 vs N=435) in patients with Irritable Bowel Syndrome with Constipation (IBS-C), the most common adverse reactions (incidence > 4%) were nausea (8% vs 4%), diarrhea (7% vs 4%), and abdominal pain (5% vs 5%).
Reduce the dosage in CIC patients with moderate and severe hepatic impairment. Reduce the dosage in IBS-C patients with severe hepatic impairment.

Please click here for complete Prescribing Information.