Possible adverse reactions are grouped according to systems and organs and frequency of occurrence: very often (≥1 / 10), often (≥1 / 100 to <1/10), infrequently (≥1 / 1000 to <1/100), rarely ( ≥1 / 10000 to <1/1000), very rarely (<1/10000).
Like any remedy, ALUSTAL "Allergen of ticks" can cause side reactions in some patients.
During treatment, both local and general adverse reactions may occur. These reactions can occur at the beginning of therapy and later in the treatment process.
Immediately stop using the drug and consult a doctor if the following symptoms occur: severe allergic reactions with the rapid development of symptoms such as severe itching or rash, shortness of breath, abdominal pain, symptoms associated with a drop in blood pressure (dizziness, fainting).
The tolerability of the dose may vary depending on the patient's condition. Pre-treatment with antiallergic drugs (for example, antihistamines) that reduce the frequency and severity of adverse reactions is possible.
Slower-type reactions of the type of serum sickness with arthralgia, myalgia, urticaria, nausea, adenopathy and fever are extremely rare and require the cessation of ASIT.
From the immune system: infrequently anaphylactic shock.
From the nervous system: often - headache; infrequently - dizziness, paresthesia.
From the side of the organ of vision: often - conjunctivitis.
From the respiratory system, organs of the chest and mediastinum: very often rhinitis; often - exacerbation of asthma, cough, dyspnea; infrequently - bronchospasm, irritation in the throat.
From the gastrointestinal tract: infrequently - pain in the abdomen, nausea.
From the skin and subcutaneous tissue: often - hives, itching, eczema, redness; infrequently - generalized itching.
General disorders and disorders at the site of administration: often - edema at the injection site, itching at the injection site, hyperemia at the injection site; infrequently - fever, peripheral edema.
Reactions at the injection site, characterized by the appearance of pruritus, edema and hyperemia about 2-3 cm in diameter, can be observed relatively often, but do not lead to a change in the treatment regimen.
Post-event application experience (frequency unknown): angioedema, edema of the larynx, wheezing, vomiting, discomfort, asthenia, arthralgia, myalgia, enlarged lymph nodes, subcutaneous nodules, granuloma.
If you experience any of the side effects listed in the manual or if you notice any other side effects not listed in the instructions, tell your doctor.