Helping your patients understand what to expect can help empower them as they move through treatment with confidence.
Counseling patients throughout the course of treatment can help keep them on track with TEPEZZA
Before they start treatment
After every infusion
“After the 3rd infusion, I started seeing steady improvement, and my eyes were feeling more comfortable."
– Lily Z., real TEPEZZA patient (compensated for her time)
In the Phase 3 study, improvement of proptosis as measured by mean change from baseline was observed as early as 6 weeks and continued to improve through Week 24.1
Review key safety considerations so you can help your patients stay informed and prepared
- Reported in ~4% of patients on TEPEZZA—most reactions were mild or moderate
- Advise patients that TEPEZZA may cause infusion reactions that can occur at any time or within 24 hours after an infusion
- Instruct patients to recognize the signs and symptoms of infusion reaction and to contact their healthcare provider immediately for signs or symptoms of potential infusion-related reactions
- In clinical trials, 10% of patients (two-thirds of whom had preexisting diabetes or impaired glucose tolerance) experienced hyperglycemia
- Assess patients for elevated blood glucose and hyperglycemia symptoms before and during treatment
- Ensure patients with hyperglycemia or preexisting diabetes are under appropriate glycemic control before and during treatment
- Monitor patients for signs and symptoms of IBD; if exacerbation is suspected, discontinue TEPEZZA
- Inform patients that inflammatory bowel disease (IBD) has been reported in some patients treated with TEPEZZA, including individuals with or without prior diagnosis of IBD
- Advise patients on the risk of IBD and to seek medical advice immediately if they experience diarrhea, with or without blood or rectal bleeding, associated with abdominal pain or cramping/colic, fecal urgency, tenesmus, or incontinence
- TEPEZZA may cause severe hearing impairment including hearing loss, which in some cases may be permanent
- Assess patients’ hearing before, during, and after treatment with TEPEZZA and consider the benefit-risk of treatment with patients
- Instruct patients to contact their healthcare provider if they experience any signs or symptoms of hearing impairment or any changes in hearing
- Advise women of childbearing potential that TEPEZZA can cause harm to a fetus and to inform their healthcare provider of a known or suspected pregnancy
- Women of childbearing potential need to use effective contraception before, during, and for 6 months after last dose
- Women of childbearing age should have a pregnancy test performed by their doctor before starting treatment with TEPEZZA
- Incidence ≥5% and greater than placebo: muscle spasm, nausea, alopecia, diarrhea, fatigue, hyperglycemia, hearing impairment, dysgeusia, headache, dry skin, ear discomfort, weight decreased, nail disorders, and menstrual disorders
"To see myself now after this treatment, it’s been uplifting because I don’t think about my eyes every day anymore. I can go about my day being confident and people aren’t asking me about my eyes or staring at my eyes.”
– Kim E., real TEPEZZA patient
(compensated for her time)