Brand Names: Stromectol
Please note – some side effects for Ivermectin may not be reported. Always consult your doctor or healthcare specialist for medical advice. You may also report side effects to the FDA at http://www.fda.gov/medwatch/ or 1-800-FDA-1088 (1-800-332-1088).
Side Effects of Ivermectin – for the Consumer
All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome when using Ivermectin:
Diarrhea; dizziness; nausea.
Seek medical attention right away if any of these SEVERE side effects occur when using Ivermectin:
Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); eye pain, swelling, or redness; fainting; fast heartbeat; fever; joint pain; red, swollen, blistered, or peeling skin; seizures; severe dizziness or lightheadedness; swelling of the skin, arms, legs, ankles, or feet; tender or swollen lymph glands (eg, in the neck, groin, underarms); vision changes; yellowing of the eyes or skin.
This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.
Side Effects by Body System – for Healthcare Professionals
Ivermectin is well tolerated compared to other microfilaricidal agents (i.e., thiabendazole, diethylcarbamazine). Adverse reactions (i.e., pruritus, fever, rash, myalgia, headache) occur commonly during the first 3 days after treatment and appear to be related to the extent of parasitic infection and systemic mobilization and killing of microfilariae. The majority of reactions can usually be treated with aspirin, acetaminophen and/or antihistamines. Adverse effects tend to occur with lesser frequency during periods of retreatment.
Ocular side effects have included eyelid edema, anterior uveitis, blurred vision, conjunctivitis, limbitis, punctate opacity, keratitis, abnormal sensation in the eyes, and chorioretinitis/choroiditis; however, these effects are also associated with the disease onchocerciasis. Loss of vision has occurred rarely but usually resolved without corticosteroid treatment. Conjunctival hemorrhage has been reported during postmarketing experience in patients treated for onchocerciasis.
Worsening of Mazzotti reactions, including arthralgia, synovitis, lymph node enlargement and tenderness, pruritus, skin involvement (including edema, papular and pustular or frank urticarial rash), and fever, has been reported during the first 4 days following treatment for onchocerciasis.
Nervous system side effects have included dizziness, headache, somnolence, vertigo, and tremor. Serious or fatal encephalopathy has been reported rarely in patients with onchocerciases, and heavily infected with Loa loa, either spontaneously or after treatment with ivermectin. Seizures have been reported during postmarketing experience.
Gastrointestinal side effects have included anorexia, constipation, diarrhea, nausea, vomiting, and abdominal distention.
Other side effects have included asthenia, fatigue, abdominal pain, chest discomfort, facial edema, and peripheral edema.
Hematologic side effects have included decreased leukocyte count (3%), eosinophilia (3%), and increased hemoglobin (1%). Hematomatous swellings associated with prolonged prothrombin times have been reported, but the clinical significance is unknown. Leukopenia and anemia have been reported in at least one patient.
Hepatic side effects have included elevated ALT and/or AST. Elevated liver enzymes, elevated bilirubin, and hepatitis have been reported during postmarketing experience.
Cardiovascular side effects have included tachycardia and orthostatic hypotension. EKG changes, including prolonged PR interval, flattened T waves and peaked T waves, have been reported in single cases. Hypotension (primarily orthostatic hypotension) has been reported during postmarketing experience.
Dermatologic side effects have included pruritus, rash, and urticaria. Toxic epidermal necrolysis and Stevens-Johnson syndrome have been reported during postmarketing experience.
Respiratory side effects have included worsening bronchial asthma, laryngeal edema, and dyspnea.
Musculoskeletal side effects have included myalgia.
Renal side effects have included rare transient proteinuria.
ALTERNATIVE: (Available for purchase at Hero’s Pets)
Azmira Giardia and Parasitic – this herbal extract supplement contains all-natural ingredients to help defend your pet’s body against a wide range of worms, amoebas, and parasites, including heartworm. Provides an excellent compound containing bitter principles, which activate digestion secretions and blood cleansing. Can be used safely to clean out the colon, even with IBS, when parasites are the suspected trigger. This extract can also be used internally, as well as topically, to address parasitic fungal and yeast growth.
Ingredients: Proprietary blend of Wormwood, Quassia Bark, Black Walnut Hulls, Neem Leaves, Bilva Herb, Embelia Ribes, Eclipta Alba, Phyllanthus Amarus, Gentian Root, Ginger Root, Grain alcohol and Spring Water.
Directions: – Give daily 6 days a week for 6 weeks. – Take the 7th week off – Repeat this cycle for 6 months – After 6 months, take a month off – After the month off, begin the cycle again if needed. – Give 1 drop per 5 pounds of body weight per dose. Can be doubled initially to build up therapeutic properties or needed for acute situations. – Give orally, mixing extract in a small amount of warm water or food. Repeat dose up to 3-4 times per day in between meals, for optimum results.
For additional product questions call 520-886-1727 or 520-293-6639 or email firstname.lastname@example.org