In clinical trials involving 109 patients given either one or two doses of 170 to 200 mcg/kg Ivert (Ivert), the following laboratory abnormalities were seen regardless of drug relationship: elevation in ALT and/or AST (2%), lower in leukocyte rely (3%). Leukopenia and anemia had been seen in one affected person. In four clinical studies involving a total of 109 patients given either one or two doses of 170 to 200 mcg/kg of Ivert (Ivert), the following adverse reactions were reported as possibly, most likely, or positively associated to Ivert (Ivert) :Body as a whole: asthenia/fatigue (0.9%), abdominal ache (0.9%)Gastrointestinal: anorexia (0.9%), constipation (0.9%), diarrhea (1.8%), nausea (1.8%), vomiting (0.9%)Nervous System/Psychiatric: dizziness (2.8%), somnolence (0.9%), vertigo (0.9%), tremor (0.9%)Skin: pruritus (2.8%), rash (0.9%), and urticaria (0.9%).In comparative trials, patients handled with Ivert (Ivert) experienced extra stromectol pills abdominal distention and chest discomfort than patients treated with albendazole.
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