The most common side effects of albendazole are experienced by over 10% of people and include
headache and abnormal liver function.
[2] Elevation of
liver enzymes occurs in 16% of patients receiving treatment specifically for hydatid disease and goes away when treatment ends.
[12][34] Liver enzymes usually increase to two to four times the normal levels (a mild to moderate increase).
[35] An estimated 1–10% of people experience
abdominal pain,
nausea or
vomiting,
dizziness or
vertigo, increased
intracranial pressure, meningeal signs, temporary
hair loss, and
fever. The headache, nausea, and vomiting are thought to be caused by the sudden destruction of
cysticerci (tapeworm larvae), which causes acute inflammation.
[36] Fewer than 1% of people get
hypersensitivity reactions such as rashes and hives,
leukopenias (drop in white blood cell levels) such as
agranulocytosis and
granulocytopenia,
thrombocytopenia (reduced platelet count),
pancytopenia (drop in white blood cells, red blood cells, and platelets),
hepatitis, acute
liver failure,
acute kidney injury, irreversible
bone marrow suppression, and
aplastic anemia.
[2][37]
Side effects can be different when treating for hydatid disease versus neurocysticercosis: for example, those being treated for the former are more likely to experience elevated liver enzymes and abdominal pain, while those being treated for the latter are more likely to experience headache.
[34] Treating hydatid disease can also unmask undiagnosed neurocysticercosis.
[34] People receiving albendazole for the treatment of neurocysticercosis can have neurological side effects such as
seizures, increased intracranial pressure, and
focal signs caused by the inflammatory reaction that occurs when parasites in the brain are killed. Steroids and anticonvulsants are often given with albendazole when treating neurocysticercosis to avoid these effects.
[34] Those being treated for retinal neurocysticercosis can face
retinal damage if they are not first checked for ocular cysticeri, since changes to existing lesions in the eye by albendazole can cause permanent blindness.
[12]
Because of its low solubility, albendazole often cannot be absorbed in high enough quantities to be toxic.
[36] The oral
LD50 of albendazole in rats was found to be 2,500 mg/kg.
[28] It takes 20 times the normal dose to kill a sheep, and 30 times the normal dose to kill cattle.
[1] Overdose affects the liver, testicles, and GI tract the most. It can manifest with lethargy, loss of appetite, vomiting, diarrhea, intestinal cramps, dizziness, convulsions, and sleepiness. There is no specified antidote.
[32