Top

If you're a returning patient or need to refill your medication, please click here.

Full Service Inhalation & Infusion Pharmacy

IV Solutions Services

IV Solutions is a division of Maxor, a National Pharmacy Services Company. Since 1986, IV Solutions has met the individual needs of people affected by complex and chronic conditions, including cystic fibrosis, bronchiolitis, immune deficiency, hemophilia, and other conditions requiring home infusion, inhalation, or speciality medications.
 
IV Solutions is accredited by the Joint Commission and services patients in all 50 states.

Read more about IV Solutions and our services>>

transfer-prescription-long

Helping Patients with Cystic Fibrosis

Cystic Fibrosis (CF) Treatments & Medications

IV Solutions is a full service Cystic Fibrosis pharmacy that provides home infusion treatments, respiratory inhalation therapies, and specialty CF medications. Since 1986, we’ve been there to help Cystic Fibrosis patients along with their families and healthcare providers.
 
IV Solutions provides limited distribution medications and devices for Cystic Fibrosis patients. These medications include: Cayston®, Bethkis®, Creon®, TOBI®, TOBI® Podhaler, Altera® Nebulizer System, Altera® Handset, and more. See full list>>
 
With IV Solutions, you’re NEVER ALONE in the fight against Cystic Fibrosis. We’re here to support you through individualized instruction, proactive refill reminders, on-going care coordination, one-on-one counseling, and clinical intervention.
 
Click below to read more our Cystic Fibrosis Services & Patient Benefits:
Cystic Fibrosis Treatment & Medications Services>>

What is Cystic Fibrosis?

Cystic Fibrosis, or CF, is a genetic disease that affects the exocrine glands. These glands control the production of sweat, digestive fluids, and mucus. Cystic Fibrosis causes the body to produce thick mucus that blocks airways, prevents normal digestive functions, and leads to bacterial infections.
 

 
 
Cystic-fibrosis-treatment-IV-Solutions

Cystic Fibrosis Facts:

  • Cystic Fibrosis is a recessive gene mutation, meaning both parents must carry the defective gene for their children to have CF.
  • Advances in newborn screening help diagnose Cystic Fibrosis at birth.
  • CF patients produce heavy mucus that builds up and damages many organs in the body.
  • In the past decade, research and medical advancements have led to an increase in life expectancy for CF patients.
  • CF is most commonly found in the Caucasian population of the United States.
  • A sweat test is the easiest way to test for CF.
  • Common symptoms and complications among CF patients include:
    • Cystic Fibrosis-Related Diabetes (CFRD)
    • Chronic sinus and lung infection
    • Gastroesophageal Reflux Disease (GERD)
    • Constant coughing; asthma, wheezing, and shortness of breath
    • Bone Disease (fracture, osteopenia or osteoporosis)

    Read more about Cystic Fibrosis>>