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Lupaneta Pack Side Effects

Generic name: leuprolide / norethindrone

Medically reviewed by Drugs.com. Last updated on Aug 21, 2023.

Note: This document contains side effect information about leuprolide / norethindrone. Some dosage forms listed on this page may not apply to the brand name Lupaneta Pack.

Applies to leuprolide / norethindrone: powder for suspension 1 month, powder for suspension 3 month, tablet.

Serious side effects of Lupaneta Pack

Along with its needed effects, leuprolide/norethindrone may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention.

Check with your doctor or nurse immediately if any of the following side effects occur while taking leuprolide / norethindrone:

More common

Incidence not known

Other side effects of Lupaneta Pack

Some side effects of leuprolide / norethindrone may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects.

Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them:

More common

Less common

For Healthcare Professionals

Applies to leuprolide / norethindrone: oral and injectable kit.

General

The most common adverse reactions leading to discontinuation of therapy included hot flashes (4%), emotional lability (4%), depression (4%) and acne (2%).

The most common adverse reaction observed were hot flashes and headaches.[Ref]

Cardiovascular

Leuprolide-Norethindrone:

Very common (10% or more): Hot flashes/sweats (up to 87%)

Leuprolide:

Very common (10% or more): Hot flashes/sweats (98%)

Postmarketing reports: Hypotension, hypertension, serious venous and arterial thrombotic and thromboembolic events (deep vein thrombosis, pulmonary embolism, myocardial infarction, stroke, transient ischemic attack[Ref]

Dermatologic

Leuprolide-Norethindrone:

Very common (10% or more): Androgen-like effects (acne, alopecia) (up to 18%), skin/mucous membrane reaction (up to 11%)

Leuprolide:

Common (1% to 10%): Androgen-like effects (acne, alopecia) (4%), skin/mucous membrane reaction (4%)[Ref]

Gastrointestinal

Leuprolide-Norethindrone:

Very common (10% or more): Altered bowel function (constipation, diarrhea) (up to 15%), nausea/vomiting (up to 29%)

Common (1% to 10%): GI disturbances (dyspepsia, flatulence) (up to 7%), changes in appetite (6%)

Leuprolide:

Very common (10% or more): Nausea/vomiting (25%), altered bowel function (constipation, diarrhea) (14%)

Common (1% to 10%): Changes in appetite (4%)%), GI disturbances (dyspepsia, flatulence) (4%)[Ref]

Genitourinary

Leuprolide-Norethindrone:

Very common (10% or more): Vaginitis (up to 15%%), breast changes/pain/tenderness (up to 13%)

Common (1% to 10%): Menstrual disorders (5%)

Frequency not reported: Urinary tract infection

Leuprolide:

Very common (10% or more): Vaginitis (20%)

Common (1% to 10%): Breast changes/pain/tenderness (6%), menstrual disorders (2%)[Ref]

Hematologic

Leuprolide:

Postmarketing reports: Decreased white blood count[Ref]

Hepatic

Leuprolide:

Postmarketing reports: Serious liver injury

Leuprolide-Norethindrone:

Common (1% to 10%): Elevated SGPT (at least twice the upper limit) (2%), elevated GGT (1.5%)[Ref]

Hypersensitivity

Leuprolide-Norethindrone:

Postmarketing reports: Allergic reactions (anaphylactic, rash, urticaria, photosensitivity)[Ref]

Local

Leuprolide-Norethindrone:

Common (1% to 10%): Injection site reaction (up to 9%)

Leuprolide:

Common (1% to 10%): Injection site reaction (2%)

Postmarketing reports: Localized reactions including induration and abscess at the site of injection[Ref]

Metabolic

Leuprolide-Norethindrone:

Very common (10% or more): Weight gain (up to 13%)

Common (1% to 10%): Edema (up to 9%), elevated SGPT (at least twice the upper limit) (2%), elevated GGT (1.5%)

Frequency not reported: Increased total cholesterol (greater than 240 mg/dL), decreased HDL cholesterol (less than 40 mg/dL), increased LDL cholesterol (greater than 160 mg/dL), increased LDL/HDL ratio (greater than 4), increased triglycerides (greater than 200 mg/dL)

Leuprolide:

Common (1% to 10%): Weight gain (12%)[Ref]

Musculoskeletal

Leuprolide:

Postmarketing reports: Spinal fracture, tenosynovitis-like symptoms, symptoms consistent with fibromyalgia[Ref]

Nervous system

Leuprolide-Norethindrone:

Very common (10% or more): Headache/migraine (up to 51%), insomnia/sleep disorders (up to 15%), dizziness/vertigo (up to 11%)

Common (1% to 10%): Neuromuscular disorder (leg cramps, paraesthesia) (up to 9%), decreased libido (up to 7%), memory disorder (up to 4%)

Leuprolide:

Very common (10% or more): Headache/migraine (65%), insomnia/sleep disorders (31%), dizziness/vertigo (16%), decreased libido (10%)

Common (1% to 10%): Memory disorder (6%), neuromuscular disorder (leg cramps, paraesthesia) (2%)

Postmarketing reports: Pituitary apoplexy, convulsion, peripheral neuropathy, paralysis[Ref]

Other

Leuprolide-Norethindrone:

Very common (10% or more): Pain (up to 29%), asthenia (up to 18%)

Leuprolide:

Very common (10% or more): Pain (24%), asthenia (18%)

Psychiatric

Leuprolide-Norethindrone:

Very common (10% or more): Depression/emotional lability (up to 34%), nervousness/anxiety (up to 11%)

Leuprolide:

Very common (10% or more): Depression/emotional lability (31%)

Common (1% to 10%): Nervousness/anxiety (8%)

Postmarketing reports: Mood swings, suicidal ideation and attempt[Ref]

Renal

Leuprolide-Norethindrone:

Frequency not reported: Renal calculus[Ref]

Respiratory

Leuprolide:

Postmarketing reports: Symptoms consistent with an asthmatic process[Ref]

References

1. Product Information. Lupaneta Pack (leuprolide-norethindrone). Abbott Pharmaceutical. 2013.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Some side effects may not be reported. You may report them to the FDA.