List of adverse effects of olanzapine

This is a list of adverse effects of the antipsychotic olanzapine, sorted by frequency of occurrence.[1]

## Contents

* 1 Very common
* 2 Common
* 3 Uncommon
* 4 Rare
* 5 Very rare (but not necessarily causally related)
* 6 References

## Very common[edit | edit source]

Very common adverse effects of olanzapine, occurring more than 10%, include:

* Weight gain (dose-dependent). Weight gain of over 7% of a person's initial body weight prior to treatment is in this category of very common too with some estimates of its incidence putting it at around 40.6%. This adverse effect is most likely the result of its potent 5-HT2C receptor and H1 receptor blockade (or more specifically inverse agonism).[2]
* Somnolence (dose-dependent). Tends to produce a moderate amount of sedation, less than clozapine and chlorpromazine but more than aripiprazole, amisulpride, paliperidone and sertindole and approximately that of quetiapine and risperidone.[3]
* Hyperprolactinemia elevated blood levels of the hormone, prolactin. Prolactin is one of the hormones that plays a key role in lactation. Long-term uncontrolled hyperprolactinaemia can lead to bone demineralisation (osteoporosis) and an increased risk of fractures (breaks). It tends to produce hyperolactinaemia less often than risperidone, paliperidone and the typical antipsychotics but more often than quetiapine and clozapine.
* Hypertriglyceridaemia (elevated blood triglycerides)
* Hypercholesterolaemia (elevated blood cholesterol levels)
* Hyperglycaemia (elevated blood glucose levels). This may be the result of olanzapine's inhibitory effects on the M3 receptor which regulates the release of insulin from the pancreas.[2]
* Brain shrinkage (dose dependent)[4][5][6][7]

## Common[edit | edit source]

Common adverse effects of olanzapine, occurring from 1-10%, include:

* Gynecomastia[8]
* Extrapyramidal symptoms (EPS) (dose-dependent). Tends to produce less extrapyramidal side effects than typical antipsychotics but more extrapyramidal side effects than sertindole, clozapine and quetiapine.[9][10]
* Mild and transient constipation and xerostomia (dry mouth)
* Dizziness
* Weight gain of over 15% of one's initial body weight. Is reported to occur in approximately 7.1% of patients.
* Glucosuria (glucose in the urine. This is a consequence of hyperglycaemia)
* Accidental injury
* Insomnia
* Orthostatic hypotension (a drop in blood pressure that occurs upon standing up)
* Transient, asymptomatic elevations of hepatic aminotransferases (ALT, AST), especially in early treatment. ALT & AST are liver enzymes which are often tested for as a measure of liver function.
* Dyspepsia (indigestion)
* Erectile dysfunction. This is most likely the result of hyperprolactinaemia.
* Decreased libido. This is most likely the result of hyperprolactinaemia.
* Rash
* Asthenia (weakness)
* Fatigue
* Oedema the accumulation of fluid in the tissues of the body leading to swelling
* Akathisia an inner sense of restlessness that presents itself with the inability to stay still
* Parkinsonism tremor, muscle rigidity, reduced ability to move and being unstable on one's feet
* Dyskinesia abnormal, involuntary, repetitive, and pointless movements
* Vomiting [11]
* Coma [12]
* Cardiac arrest [13]

## Uncommon[edit | edit source]

Uncommon adverse effects of olanzapine, occurring from 0.1-1%, include:

* Leukopaenia a comparatively low white blood cell (the cells that defend the body from foreign invaders) count.
* Neutropaenia a reduced neutrophil (the white blood cells that kill bacteria) count.
* Bradycardia (low heart rate)
* QTc interval prolongation (an abnormality in the electrical cycle of the heart)
* Photosensitivity reaction
* Alopecia (hair loss)
* Urinary incontinence
* Urinary retention, the inability to urinate.
* Amenorrhea the cessation of menses (a woman's menstrual cycles). This is a complication of hyperprolactinaemia.
* Breast enlargement (in either sex). This is a complication of hyperprolactinaemia.
* Galactorrhoea (expulsion of milk from the breasts that's unrelated to pregnancy or lactation. Most likely the result of hyperprolactinaemia)
* High creatine phosphokinase (an abnormal laboratory finding)
* Increased total bilirubin (a by product of the breakdown of haem - a part of blood cells that is used to carry oxygen. In most people this is an indication of impaired liver function)
* Abdominal pain [14]

## Rare[edit | edit source]

Rare adverse effects of olanzapine, occurring from 0.01-0.1%, include:

* Hepatitis
* Rash
* Seizures
* Glaucoma [15]
* Blindness [16]

## Very rare (but not necessarily causally related)[edit | edit source]

Very rare adverse effects of olanzapine, occurring less than 0.01%, include:

* Agranulocytosis, a potentially fatal drop in white blood cell count, basically an exaggerated form of leukopaenia.
* Thrombocytopaenia. A drop in blood platelet counts which are involved in blood clotting.
* Thromboembolism (blood clots; including pulmonary embolism and deep vein thrombosis)
* Rhabdomyolysis (breakdown of muscle tissue leading to the release of myoglobin into the bloodstream which in turn damages the kidneys)
* Alkaline phosphatase increased (an abnormal laboratory parameter)
* Priapism (a painful and enduring erection)
* Urinary hesitation
* Pancreatitis, swelling of the pancreas which supplies the body with insulin.
* Neuroleptic malignant syndrome a potentially fatal complication of antipsychotic drug treatment. Presents with hyperthermia, tremor, tachycardia (high heart rate), mental status change (e.g. confusion), etc.
* Jaundice, which is basically when the body's ability to clear a by product (called bilirubin) of the breakdown of an essential component of the blood called haem, is impaired leading to yellow discolouration of the skin, eyes and mucous membranes.
* Diabetic coma
* Diabetic ketoacidosis. Type II diabetes mellitus is basically where the body cannot effectively utilise sugars to produce energy due to the fact that its cells have become unresponsive to the hormone, insulin, which allows cells to utilise sugars for energy. This in turn forces the body to burn fats for energy and fats require conversion to ketone bodies in order to be utilised by the cells of the body as an energy source. The ketone bodies are acidic hence when the body is entirely reliant on these ketone bodies for energy the levels in the blood reaches a point where it overwhelms the body's natural mechanisms to keep blood pH (a measure of acidity) within a safe range, leading to the blood becoming acidic which is potentially damaging to the tissues of the body due to the ability of acidic environments to denature the proteins of the body.
* Anaphylactic reaction a potentially life-threatening allergic reaction
* Sudden cardiac death

## References[edit | edit source]

1. ↑ Lexi-Comp Inc. (2010) Lexi-Comp Drug Information Handbook 19th North American Ed. Hudson, OH: Lexi-Comp Inc. ISBN 978-1-59195-278-7.
2. ↑ 2.0 2.1 Brunton, L; Chabner, B; Knollman, B (2010). Goodman and Gilman's The Pharmacological Basis of Therapeutics (12th ed.). New York: McGraw-Hill Professional. ISBN 978-0-07-162442-8.
3. ↑ Leucht, S; Cipriani, A; Spineli, L; Mavridis, D; Örey, D; Richter, F; et al. (Sep 2013). "Comparative efficacy and tolerability of 15 antipsychotic drugs in schizophrenia: a multiple-treatments meta-analysis". The Lancet. 382 (9896): 951–62. doi:10.1016/S0140-6736(13)60733-3. PMID 23810019. S2CID 32085212.
4. ↑ Moncrieff, J.; Leo, J. (September 2010). "A systematic review of the effects of antipsychotic drugs on brain volume". Psychological Medicine. 40 (9): 1409–1422. doi:10.1017/S0033291709992297. PMID 20085668. S2CID 23522488.
5. ↑ Ho, Beng-Choon; Andreasen, Nancy C.; Ziebell, Steven; Pierson, Ronald; Magnotta, Vincent (7 February 2011). "Long-term Antipsychotic Treatment and Brain Volumes: A Longitudinal Study of First-Episode Schizophrenia". Archives of General Psychiatry. 68 (2): 128–137. doi:10.1001/archgenpsychiatry.2010.199. PMC 3476840. PMID 21300943.
6. ↑ Fusar-Poli, P.; Smieskova, R.; Kempton, M.J.; Ho, B.C.; Andreasen, N.C.; Borgwardt, S. (September 2013). "Progressive brain changes in schizophrenia related to antipsychotic treatment? A meta-analysis of longitudinal MRI studies". Neuroscience & Biobehavioral Reviews. 37 (8): 1680–1691. doi:10.1016/j.neubiorev.2013.06.001. PMC 3964856. PMID 23769814.
7. ↑ Voineskos, Aristotle N.; Mulsant, Benoit H.; Dickie, Erin W.; Neufeld, Nicholas H.; Rothschild, Anthony J.; Whyte, Ellen M.; Meyers, Barnett S.; Alexopoulos, George S.; Hoptman, Matthew J.; Lerch, Jason P.; Flint, Alastair J. (1 July 2020). "Effects of Antipsychotic Medication on Brain Structure in Patients With Major Depressive Disorder and Psychotic Features: Neuroimaging Findings in the Context of a Randomized Placebo-Controlled Clinical Trial". JAMA Psychiatry. 77 (7): 674–683. doi:10.1001/jamapsychiatry.2020.0036. PMC 7330722. PMID 32101271.
8. ↑ "Olanzapine-Induced Gynecomastia". Australian & New Zealand Journal of Psychiatry. 39 (8): 736. August 2005. doi:10.1080/j.1440-1614.2005.01666_1.x. S2CID 208625245.
9. ↑ Taylor, D. The Maudsley prescribing guidelines in psychiatry. Wiley-Blackwell.
10. ↑ Rossi, S, ed. (2013). Australian Medicines Handbook (2013 ed.). Adelaide: The Australian Medicines Handbook Unit Trust. ISBN 978-0-9805790-9-3.
11. ↑ "Olanzapine and Vomiting, a phase IV clinical study of FDA data - eHealthMe". Archived from the original on 2011-09-17. Retrieved 2021-08-04.
12. ↑ "Olanzapine and Coma, a phase IV clinical study of FDA data - eHealthMe". Archived from the original on 2022-01-28. Retrieved 2021-08-04.
13. ↑ "Olanzapine and Cardiac arrest, a phase IV clinical study of FDA data - eHealthMe". Archived from the original on 2022-01-28. Retrieved 2021-08-04.
14. ↑ "Olanzapine and Abdominal pain, a phase IV clinical study of FDA data - eHealthMe". Archived from the original on 2022-01-28. Retrieved 2021-08-04.
15. ↑ "Olanzapine and Glaucoma, a phase IV clinical study of FDA data - eHealthMe". Archived from the original on 2022-01-28. Retrieved 2021-08-04.
16. ↑ "Olanzapine and Blindness, a phase IV clinical study of FDA data - eHealthMe". Archived from the original on 2022-01-28. Retrieved 2021-08-04.