Lithonate Side Effects
Generic Name: lithium
Note: This document contains side effect information about lithium. Some of the dosage forms listed on this page may not apply to the brand name Lithonate.
For the Consumer
Applies to lithium: oral capsule, oral solution, oral syrup, oral tablet, oral tablet extended release
Along with its needed effects, lithium (the active ingredient contained in Lithonate) may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention.
Check with your doctor immediately if any of the following side effects occur while taking lithium:
- Confusion, poor memory, or lack of awareness
- fast or slow heartbeat
- frequent urination
- increased thirst
- irregular pulse
- stiffness of the arms or legs
- troubled breathing (especially during hard work or exercise)
- unusual tiredness or weakness
- weight gain
- Blue color and pain in the fingers and toes
- coldness of the arms and legs
- eye pain
- noise in the ears
- vision problems
Incidence not known
- Dry, rough skin
- fast, irregular, pounding, or racing heartbeat or pulse
- hair loss
- mental depression
- sensitivity to cold
- shortness of breath
- swelling of the feet or lower legs
- swelling of the neck
- unusual excitement
Get emergency help immediately if any of the following symptoms of overdose occur while taking lithium:
Symptoms of overdose
- Blurred vision
- clumsiness or unsteadiness
- convulsions (seizures)
- increase in the amount of urine
- lack of coordination
- loss of appetite
- muscle weakness
- nausea or vomiting
- ringing in the ears
- slurred speech
- trembling (severe)
Some side effects of lithium may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects. Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them:
For Healthcare Professionals
Applies to lithium: compounding powder, oral capsule, oral syrup, oral tablet, oral tablet extended release
Frequency not reported: Abnormal reflex convulsions, acute dystonia, ataxia, benign intracranial hypertension, blackout spells, choreoathetotic movements, cerebellar syndrome, clonic movements of whole limbs, coarse tremor of the extremities and lower jaw, cogwheel rigidity, coma, convulsions, diffuse slowing of EEG, dizziness, downbeat nystagmus, drowsiness, dysarthria, dysgeusia/taste distortion, encephalopathy, encephalopathic syndrome, epileptiform seizures, extrapyramidal syndrome, fine hand tremor, giddiness, headache, hyperactive deep tendon reflexes, hypertonicity, impaired consciousness, lack of coordination, lethargy, metallic/salty taste, myoclonus, nystagmus, peripheral sensorimotor neuropathy, poor memory, potentiation and disorganization of EEG background rhythm, pseudotumor cerebri (increased intracranial pressure and papilledema), psychomotor retardation, seizures, serotonin syndrome, slowed intellectual functioning, slurred speech/speech disorder, somnolence, startle response, stupor, tendency to sleep, tongue movements, transient electroencephalogram (EEG), tremor, vertigo, widening of EEG frequency spectrum[Ref]
Drowsiness and lack of coordination may be early signs of lithium toxicity, and may occur at lithium levels below 2 mEq/L.
Ataxia and giddiness occurred at levels above 2 mEq/L.
Fine hand tremor may occur during initial therapy for the acute manic phase, and may persist during therapy.
The development of transient EEG changes, headache, dysgeusia/taste distortion, and metallic taste were unrelated to dosage.
Peripheral neuropathy may occur in patients on long-term treatment, but is usually reversible after discontinuation of therapy.[Ref]
The development of transient ECG changes, chest tightness, and edematous swelling of ankles/wrists were unrelated to dosage.
Painful discoloration of the fingers/toes and coldness of extremities (resembling Raynaud's syndrome) occurred within one day of initiation; the patient recovered after discontinuation. The exact mechanism for this side effect is unknown.[Ref]
Frequency not reported: Atrioventricular block, bradycardia, cardiac arrhythmia, cardiomyopathy, chest tightness, conduction disturbance, ECG changes, edema, hypotension, inversion of T-waves, isoelectricity of ECG, peripheral circulatory collapse, peripheral edema/edematous swelling of ankles or wrists, peripheral vasculopathy, QT prolongation, Raynaud's phenomena/syndrome, reversible flattening of ECG, sinus node dysfunction with severe bradycardia and/or sinoatrial block (may result in syncope), transient ECG changes, unmasking of Brugada syndrome, ventricular tachyarrhythmia[Ref]
Frequency not reported: Abdominal pain/discomfort, constipation, dental caries, diarrhea, dry mouth, excessive salivation, flatulence, gastritis, incontinence of feces, indigestion, nausea/transient and mild nausea, salivary gland swelling, swollen lips, vomiting[Ref]
Diarrhea and vomiting may be early signs of lithium toxicity, and may occur at lithium levels below 2 mEq/L.
Transient and mild nausea may occur within the first few days of therapy.
The development of metallic/salty taste, dental caries, and swollen lips were unrelated to dosage.[Ref]
Frequency not reported: Acne/acneform eruptions, alopecia, anesthesia of skin, chronic folliculitis/folliculitis, cutaneous ulcers, drying and thinning of hair, generalized pruritus with/without rash, papular skin disorders, pruritus, psoriasis onset/exacerbation, urticaria, xerosis cutis[Ref]
The development of generalized pruritus with/without rash and cutaneous ulcers were unrelated to dosage.[Ref]
Frequency not reported: Diffuse nontoxic goiter with/without hypothyroidism, euthyroid goiter, hyperparathyroidism, hyperthyroidism, hypothyroidism (including myxedema), iodine 131 uptake increased, lower T3 and T4 levels, thyrotoxicosis[Ref]
Hyperthyroidism has been rarely reported, and may persist after discontinuation of treatment.
Hyperparathyroidism may persist after discontinuation of treatment.
The development of diffuse nontoxic goiter with/without hypothyroidism and hyperparathyroidism were unrelated to dosage.[Ref]
Muscular weakness develops early in lithium (the active ingredient contained in Lithonate) toxicity, and may occur at lithium levels below 2 mEq/L.
Muscle hyperirritability includes fasciculations, twitching, clonic movements of whole limbs.
The development of swollen/painful joints and polyarthralgia were unrelated to dosage.[Ref]
Frequency not reported: Decreased creatinine clearance, glycosuria, histological renal changes with interstitial fibrosis, lithium-induced chronic kidney disease, microcysts, nephrogenic diabetes insipidus, nephrotic syndrome, oliguria, renal dysfunction[Ref]
Diabetes insipidus may persist after discontinuation of treatment.
Histological renal changes with interstitial fibrosis occurred in patients on prolonged treatment, and was usually reversible upon discontinuation. Long-term treatment may cause permanent kidney changes and impairment of renal function; high serum concentrations and/or acute lithium toxicity may worsen these changes.[Ref]
Frequency not reported: Anorexia, dehydration, excessive weight gain, hypercalcemia, hypermagnesemia, hyponatremia, polydipsia, thirst/mild thirst, transient hyperglycemia/hyperglycemia, weight loss[Ref]
The development of transient hyperglycemia, hypercalcemia, and excessive weight gain were unrelated to dosage.[Ref]
Tinnitus occurred at levels above 2 mEq/L.
Mild thirst may occur during initial therapy for the acute manic phase, and may persist during therapy; in some cases, thirst resembled diabetes insipidus. The development of thirst was unrelated to dosage.
General discomfort may also appear within the first few days of therapy.
The development of fever was unrelated to dosage.[Ref]
Frequency not reported: Fall, fasciculations, fatigue, feeling dazed, fever, general discomfort, lithium toxicity, tinnitus[Ref]
At levels above 2 mEq/L, patients excreted a large output of dilute urine.
Polyuria may occur during initial therapy for the acute manic phase, and may persist during therapy; in some cases, polyuria resembled diabetes insipidus. The development of polyuria was unrelated to dosage.
The development of albuminuria was unrelated to dosage.[Ref]
Frequency not reported: Confusion, delirium, hallucinations, restlessness, tics, worsening of organic brain syndromes[Ref]
The worsening of organic brain syndromes was unrelated to dosage.[Ref]
Frequency not reported: Blindness, blurred vision, enlargement of the blind spot, exophthalmos, optic atrophy, transient scotomata/scotoma, visual field constriction[Ref]
Blurred vision occurred at levels above 2 mEq/L.[Ref]
Frequency not reported: Collecting duct renal carcinoma, oncocytoma[Ref]
Collecting duct renal carcinoma occurred in patients on long-term therapy.[Ref]
The development of leukocytosis was unrelated to dosage.[Ref]
1. "Product Information. Lithobid (lithium)." Ciba Pharmaceuticals, Summit, NJ.
2. Cerner Multum, Inc. "UK Summary of Product Characteristics." O 0
3. "Product Information. Eskalith (lithium)." SmithKline Beecham, Philadelphia, PA.
4. Cerner Multum, Inc. "Australian Product Information." O 0
5. Therapeutic Goods Administration (TGA) "Medicines Safety Update, Volume 8 Number 4, August-September 2017 Available from: URL: https://www.tga.gov.au/publication-issue/medicines-safety-update-volume-8-number-4-august-september-2017" ([2017, Sep 17]):
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.
Some side effects may not be reported. You may report them to the FDA.
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