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Home > Drugs > Corticotropin > Acthar gel, h.p. > Acthar gel, h.p. Side Effects
Corticotropin

H.P. Acthar Gel Side Effects

Note: This document contains side effect information about corticotropin. Some dosage forms listed on this page may not apply to the brand name H.P. Acthar Gel.

Applies to corticotropin: parenteral solution for injection.

Side effects include:

Associated with long-term therapy: Bone loss, cataracts, indigestion, muscle weakness, back pain, bruising, acne, hyperpigmentation, menstrual irregularities, oral candidiasis. (See Warnings/Precautions under Cautions.)

For Healthcare Professionals

Applies to corticotropin: injectable powder for injection, injectable solution.

General

The more commonly reported adverse effects have included fluid retention, changes in glycemic control, increased appetite and weight gain; for children less than 2 years, increased risk of infections, hypertension, irritability, Cushingoid symptoms, cardiac hypertrophy, and weight gain have been reported.[Ref]

Cardiovascular

The incidence of cardiac hypertrophy in patients less than 2 years treated for infantile spasm was 3% for patients receiving 75 units/m2 twice a day and 0% for those receiving 150 units/m2/day based on retrospective chart reviews and clinical trials. For hypertension, the incidence of was 11% for patients receiving 75 units/m2 twice a day and 19% for those receiving 150 units/m2/day.

Very Common (10% or more): Hypertension

Common (1% to 10%): Cardiac hypertrophy

Frequency not reported: Fluid retention

Postmarketing reports: Necrotizing angitis (adults only), congestive heart failure

Nervous system

In the treatment of infantile spasms, other types of seizures/convulsions may occur because some patients progress to other forms of seizures such as Lennox-Gastaut syndrome and because spasms may be masking other seizures. The incidence of seizure was 12% for patients receiving 75 units/m2 twice a day and 3% for those receiving 150 units/m2/day based on retrospective chart reviews and clinical trials.

Very Common (10% to more): Convulsions

Postmarketing reports: Headache (adults only), subdural hematoma, intracranial hemorrhage (adults only), reversible brain shrinkage (secondary to hypertension; infants only)

Psychiatric

Common (1% to 10%): Irritability

Frequency not reported: Behavioral and mood changes

Metabolic

Common (1% to 10%): Increased appetite, decreased appetite, weight gain

Frequency not reported: Alteration in glucose tolerance

Postmarketing reports: Hypokalemic alkalosis (infants only), decreased carbohydrate tolerance (infants only)

Dermatologic

The incidence of acne and rash in patients less than 2 years treated for infantile spasm was 0% for patients receiving 75 units/m2 twice a day and 12% and 8%, respectively for those receiving 150 units/m2/day based on retrospective chart reviews and clinical trials.

Very common (10% or more): Acne

Common (1% to 10%): Rash

Postmarketing reports: Skin thinning (adults only), facial erythema, increased sweating (adults only), hirsutism

Local

Postmarketing reports: Injection site reactions

Musculoskeletal

Postmarketing reports: Muscle weakness and vertebral compression fractures (infants only)

Endocrine

The incidence of Cushingoid in patients less than 2 years treated for infantile spasm was 3% for patients receiving 75 units/m2 twice a day and 22% for those receiving 150 units/m2/day based on retrospective chart reviews and clinical trials.

Common (1% to 10%): Cushingoid

Gastrointestinal

Very common (10% or more): Diarrhea

Common (1% to 10%): Constipation, diarrhea, vomiting

Postmarketing reports: Pancreatitis (adults only), abdominal distention, ulcerative esophagitis

Hypersensitivity

Postmarketing reports: Allergic responses presenting as dizziness, nausea, and shock (adults only)

Other

Very Common (10% or more): Infection

Common (1% or 10%): Pyrexia, candidiasis, otitis media, vertigo (adults only)

Respiratory

Common (1% or 10%): Nasal congestion, pneumonia, upper respiratory infections.

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