Lithium Carbonate interactions
Full monograph for Lithium CarbonateCheck it against another medicine
Medicines
505 documented
| Medicine | Severity | Mechanism | Effect | Sources |
|---|---|---|---|---|
| Adefovir Dipivoxil | Major | Excretion | Coadministration of adefovir dipivoxil with other nephrotoxic agents may increase the risk and severity of renal impairment due to additive effects on the… | 1 sources — open the full entry |
| Amiodarone Hydrochloride | Major | Synergy | Class IA (e.g., disopyramide, quinidine, procainamide) and class III (e.g., amiodarone, dofetilide, sotalol) antiarrhythmic agents can cause dose-related… | 45 sources — open the full entry |
| Amisulpride | Major | Synergy | Amisulpride can cause dose- and concentration-dependent prolongation of the QT interval. Theoretically, coadministration with other agents that can prolong the… | 3 sources — open the full entry |
| Amlodipine Besilate + Benazepril Hydrochloride | Major | Excretion · Others | Coadministration with angiotensin converting enzyme (ACE) inhibitors may increase serum lithium concentrations and the risk for lithium toxicity. Several…2 documented mechanisms | 47 sources — open the full entry |
| Amlodipine Besilate + Olmesartan Medoxomil | Major | Excretion · Others | Concomitant use of angiotensin II receptor antagonists may increase the serum concentrations of lithium. The exact mechanism of interaction is unknown, but…2 documented mechanisms | 43 sources — open the full entry |
| Amlodipine Besilate + Telmisartan | Major | Excretion · Others | Concomitant use of angiotensin II receptor antagonists may increase the serum concentrations of lithium. The exact mechanism of interaction is unknown, but…2 documented mechanisms | 43 sources — open the full entry |
| Amlodipine Besilate + Valsartan | Major | Excretion · Others | Concomitant use of angiotensin II receptor antagonists may increase the serum concentrations of lithium. The exact mechanism of interaction is unknown, but…2 documented mechanisms | 43 sources — open the full entry |
| Arsenic Trioxide | Major | Synergy | Arsenic trioxide can cause QT interval prolongation and complete atrioventricular block. Theoretically, coadministration with other agents that can prolong the… | 4 sources — open the full entry |
| Artemether + Lumefantrine | Major | Synergy | Artemether-lumefantrine may cause prolongation of the QT interval. Theoretically, coadministration with other agents that can prolong the QT interval may…2 documented mechanisms | 16 sources — open the full entry |
| Atenolol + Chlorthalidone | Major | Excretion · Synergy | Thiazide diuretics may cause a rapid increase in serum lithium levels and potentiate the risk of lithium toxicity. The exact mechanism is unknown but may be…2 documented mechanisms | 37 sources — open the full entry |
| Azilsartan Medoxomil | Major | Excretion · Others | Concomitant use of angiotensin II receptor antagonists may increase the serum concentrations of lithium. The exact mechanism of interaction is unknown, but…2 documented mechanisms | 27 sources — open the full entry |
| Azilsartan Medoxomil + Chlorthalidone | Major | Excretion · Others | Thiazide diuretics may cause a rapid increase in serum lithium levels and potentiate the risk of lithium toxicity. The exact mechanism is unknown but may be…3 documented mechanisms | 53 sources — open the full entry |
| Bisoprolol Fumarate + Hydrochlorothiazide | Major | Excretion · Synergy | Thiazide diuretics may cause a rapid increase in serum lithium levels and potentiate the risk of lithium toxicity. The exact mechanism is unknown but may be…2 documented mechanisms | 37 sources — open the full entry |
| Bromfenac Sodium | Major | Excretion | Coadministration with nonsteroidal anti-inflammatory drugs (NSAIDs) may increase serum lithium levels and induce toxicity in some patients. The exact mechanism… | 48 sources — open the full entry |
| Bumetanide | Major | Excretion | Loop diuretics may increase serum lithium levels and potentiate the risk of lithium toxicity. The exact mechanism is unknown but may be related to the sodium… | 17 sources — open the full entry |
| Bupropion Hydrochloride | Major | Synergy | The use of bupropion is associated with a dose-related risk of seizures. The risk may be further increased when coadministered with selective serotonin… | 19 sources — open the full entry |
| Cabozantinib | Major | Synergy | Cabozantinib can cause prolongation of the QT interval. | 7 sources — open the full entry |
| Candesartan Cilexetil | Major | Others | Concomitant use of angiotensin II receptor antagonists may increase the serum concentrations of lithium. The exact mechanism of interaction is unknown, but… | 10 sources — open the full entry |
| Candesartan Cilexetil + Hydrochlorothiazide | Major | Excretion · Others | Thiazide diuretics may cause a rapid increase in serum lithium levels and potentiate the risk of lithium toxicity. The exact mechanism is unknown but may be…2 documented mechanisms | 36 sources — open the full entry |
| Captopril | Major | Excretion | Coadministration with angiotensin converting enzyme (ACE) inhibitors may increase serum lithium concentrations and the risk for lithium toxicity. Several… | 21 sources — open the full entry |
| Ceritinib | Major | Synergy | Ceritinib can cause concentration-dependent prolongation of the QT interval. Theoretically, coadministration with other agents that can prolong the QT interval… | 9 sources — open the full entry |
| Chloroquine Phosphate | Major | Synergy | Chloroquine and hydroxychloroquine can cause dose-related prolongation of the QT interval. Theoretically, coadministration with other agents that can prolong… | 22 sources — open the full entry |
| Chlorthalidone | Major | Excretion | Thiazide diuretics may cause a rapid increase in serum lithium levels and potentiate the risk of lithium toxicity. The exact mechanism is unknown but may be… | 26 sources — open the full entry |
| Citalopram Hydrobromide | Major | Synergy | Lithium may enhance the pharmacologic effects of selective serotonin reuptake inhibitors (SSRIs) and potentiate the risk of serotonin syndrome, which is a rare… | 23 sources — open the full entry |
| Clozapine | Major | Synergy | Clozapine has the potential to prolong QT interval of the electrocardiogram. Theoretically, coadministration with other agents that can cause QT prolongation… | 13 sources — open the full entry |
| Crizotinib | Major | Synergy | Crizotinib can cause concentration-dependent prolongation of the QT interval. Theoretically, coadministration with other agents that can prolong the QT… | 6 sources — open the full entry |
| Deferasirox | Major | Synergy | Theoretical concerns exist regarding the potential for increased risk of renal impairment during coadministration of deferasirox with other nephrotoxic agents… | 3 sources — open the full entry |
| Desvenlafaxine Succinate | Major | Synergy | Lithium may enhance the pharmacologic effects of serotonin reuptake inhibitors (e.g., SSRIs, SNRIs, nefazodone, trazodone) and potentiate the risk of serotonin… | 22 sources — open the full entry |
| Dexibuprofen | Major | Excretion | Coadministration with nonsteroidal anti-inflammatory drugs (NSAIDs) may increase serum lithium levels and induce toxicity in some patients. The exact mechanism… | 48 sources — open the full entry |
| Dexketoprofen | Major | Excretion | Coadministration with nonsteroidal anti-inflammatory drugs (NSAIDs) may increase serum lithium levels and induce toxicity in some patients. The exact mechanism… | 48 sources — open the full entry |
| Dextromethorphan + Bupropion | Major | Synergy | The use of bupropion is associated with a dose-related risk of seizures. The risk may be further increased when coadministered with selective serotonin…2 documented mechanisms | 63 sources — open the full entry |
| Diclofenac Diethylamine + Mephenesin + Menthol + Methyl Salicylate + Turpentine Oil | Major | Excretion | Coadministration with nonsteroidal anti-inflammatory drugs (NSAIDs) may increase serum lithium levels and induce toxicity in some patients. The exact mechanism… | 48 sources — open the full entry |
| Diclofenac Potassium | Major | Excretion | Coadministration with nonsteroidal anti-inflammatory drugs (NSAIDs) may increase serum lithium levels and induce toxicity in some patients. The exact mechanism… | 48 sources — open the full entry |
| Diclofenac Sodium | Major | Excretion | Coadministration with nonsteroidal anti-inflammatory drugs (NSAIDs) may increase serum lithium levels and induce toxicity in some patients. The exact mechanism… | 48 sources — open the full entry |
| Diclofenac Sodium + Lidocaine Hydrochloride | Major | Excretion | Coadministration with nonsteroidal anti-inflammatory drugs (NSAIDs) may increase serum lithium levels and induce toxicity in some patients. The exact mechanism… | 48 sources — open the full entry |
| Diclofenac Sodium + Methyl Salicylate + Linseed Oil + Menthol | Major | Excretion | Coadministration with nonsteroidal anti-inflammatory drugs (NSAIDs) may increase serum lithium levels and induce toxicity in some patients. The exact mechanism… | 48 sources — open the full entry |
| Diclofenac Sodium + Misoprostol | Major | Excretion | Coadministration with nonsteroidal anti-inflammatory drugs (NSAIDs) may increase serum lithium levels and induce toxicity in some patients. The exact mechanism… | 48 sources — open the full entry |
| Duloxetine Hydrochloride | Major | Synergy | Lithium may enhance the pharmacologic effects of serotonin reuptake inhibitors (e.g., SSRIs, SNRIs, nefazodone, trazodone) and potentiate the risk of serotonin… | 22 sources — open the full entry |
| Efavirenz | Major | Metabolism | Efavirenz can cause significant QT interval prolongation in patients with the CYP450 2B6 *6/*6 genotype due to reduced metabolic clearance of the drug stemming… | 6 sources — open the full entry |
| Enalapril Maleate | Major | Excretion | Coadministration with angiotensin converting enzyme (ACE) inhibitors may increase serum lithium concentrations and the risk for lithium toxicity. Several… | 21 sources — open the full entry |
| Escitalopram Oxalate | Major | Synergy | Escitalopram can cause dose-dependent prolongation of the QT interval. Theoretically, coadministration with other agents that can prolong the QT interval may… | 13 sources — open the full entry |
| Etodolac | Major | Excretion | Coadministration with nonsteroidal anti-inflammatory drugs (NSAIDs) may increase serum lithium levels and induce toxicity in some patients. The exact mechanism… | 48 sources — open the full entry |
| Everolimus | Major | Synergy | Coadministration of macrolide immunosuppressants with other nephrotoxic agents may increase the risk and/or severity of renal impairment due to additive… | 4 sources — open the full entry |
| Fluoxetine Hydrochloride | Major | Synergy | Lithium may enhance the pharmacologic effects of selective serotonin reuptake inhibitors (SSRIs) and potentiate the risk of serotonin syndrome, which is a rare… | 28 sources — open the full entry |
| Flurbiprofen | Major | Excretion | Coadministration with nonsteroidal anti-inflammatory drugs (NSAIDs) may increase serum lithium levels and induce toxicity in some patients. The exact mechanism… | 48 sources — open the full entry |
| Fluvoxamine Maleate | Major | Synergy | Lithium may enhance the pharmacologic effects of selective serotonin reuptake inhibitors (SSRIs) and potentiate the risk of serotonin syndrome, which is a rare… | 28 sources — open the full entry |
| Furosemide | Major | Excretion | Loop diuretics may increase serum lithium levels and potentiate the risk of lithium toxicity. The exact mechanism is unknown but may be related to the sodium… | 17 sources — open the full entry |
| Furosemide + Spironolactone | Major | Excretion · Metabolism | Spironolactone and triamterene may increase serum lithium levels, resulting in a high risk of lithium toxicity. The mechanism is reduced renal clearance of…2 documented mechanisms | 27 sources — open the full entry |
| Gatifloxacin | Major | Synergy | Certain quinolones, including gatifloxacin and moxifloxacin, may cause dose-related prolongation of the QT interval in some patients. Theoretically… | 28 sources — open the full entry |
| Gatifloxacin + Dexamethasone | Major | Synergy | Certain quinolones, including gatifloxacin and moxifloxacin, may cause dose-related prolongation of the QT interval in some patients. Theoretically… | 28 sources — open the full entry |
Food & lifestyle
alcohol
ModerateSynergy
Alcohol may potentiate some of the pharmacologic effects of CNS-active agents. Use in combination may result in additive central nervous system depression and/or impairment of judgment, thinking, and psychomotor skills.
What to do: Patients receiving CNS-active agents should be warned of this interaction and advised to avoid or limit consumption of alcohol. Ambulatory patients should be counseled to avoid hazardous activities requiring complete mental alertness and motor coordination until they know how these agents affect them, and to notify their physician if they experience excessive or prolonged CNS effects that interfere with their normal activities.
4 sources
- Warrington SJ, Ankier SI, Turner P "Evaluation of possible interactions between ethanol and trazodone or amitriptyline." Neuropsychobiology 15 (1986): 31-7
- Gilman AG, eds., Nies AS, Rall TW, Taylor P "Goodman and Gilman's the Pharmacological Basis of Therapeutics." New York, NY: Pergamon Press Inc. (1990):
- "Product Information. Fycompa (perampanel)." Eisai Inc (2012):
- "Product Information. Rexulti (brexpiprazole)." Otsuka American Pharmaceuticals Inc (2015):
Conditions
Conditions in which Lithium Carbonate needs care, as documented in this source.
Dehydration
MajorLithium reduces the ability of the kidney to concentrate urine and produces a mild diabetes insipidus and polyuria. Therefore, patients with preexisting dehydration are more prone to lithium retention and toxicity. Therapy with lithium should be administered cautiously in dehydrated patients and may need to be discontinued until improvement in hydration status. Careful monitoring of lithium levels are recommended. Patients with sweating, diarrhea or concomitant infection with fever may need a temporary reduction or cessation of medication.
3 sources
- "Product Information. Eskalith (lithium)." SmithKline Beecham (2002):
- "Product Information. Lithobid (lithium)." Ciba-Geigy Pharmaceuticals (2002):
- Martinez EJ, Sinnott JT, 4th Rodriguez-Paz G, Oehler RL "Lithium-induced nephrogenic diabetes insipidus treated with indomethacin." South Med J 86 (1993): 971-3
Dementia
MajorOlder patients with dementia-related psychosis treated with antipsychotic drugs are at an increased risk of death; although the causes were varied, most of the deaths appeared to be either cardiovascular (e.g., heart failure, sudden death) or infectious (e.g., pneumonia) in nature. A causal relationship with antipsychotic use has not been established. In controlled trials in older patients with dementia-related psychosis, patients randomized to risperidone, aripiprazole, and olanzapine had higher incidence of cerebrovascular adverse events (e.g., stroke, transient ischemic attack), including fatalities, compared to patients treated with placebo. These agents are not approved for the treatment of patients with dementia-related psychosis.
14 sources
- "Product Information. Clozaril (clozapine)." Novartis Pharmaceuticals (2001):
- "Product Information. Risperdal (risperidone)." Janssen Pharmaceuticals (2001):
- "Product Information. Zyprexa (olanzapine)." Lilly, Eli and Company (2001):
- "Product Information. Seroquel (quetiapine)." Astra-Zeneca Pharmaceuticals (2001):
- "Product Information. Geodon (ziprasidone)." Pfizer U.S. Pharmaceuticals (2001):
- "Product Information. Abilify (aripiprazole)." Bristol-Myers Squibb (2002):
- "Product Information. Invega (paliperidone)." Janssen Pharmaceuticals (2007):
- "Product Information. Fanapt (iloperidone)." Vanda Pharmaceuticals Inc (2009):
Show all 14 sourcesShow fewer sources
- "Product Information. Saphris (asenapine)." Schering-Plough Corporation (2009):
- "Product Information. Latuda (lurasidone)." Sunovion Pharmaceuticals Inc (2010):
- "Product Information. Rexulti (brexpiprazole)." Otsuka American Pharmaceuticals Inc (2015):
- "Product Information. Vraylar (cariprazine)." Actavis Pharma, Inc. (2015):
- "Product Information. Nuplazid (pimavanserin)." Accelis Pharma (2016):
- "Product Information. Caplyta (lumateperone)." Intra-Cellular Therapies, Inc. (2022):
Diarrhea
MajorThe risk for lithium toxicity may be increased in patients with diarrhea and excessive sweating. Dehydration and sodium depletion may occur in these patients leading to lithium retention and toxicity. The use of lithium may need to be reduced or suspended until the condition resolves. Supplemental fluid and salt may need to be administered. Monitoring serum lithium levels is recommended.
2 sources
- "Product Information. Eskalith (lithium)." SmithKline Beecham (2002):
- "Product Information. Lithobid (lithium)." Ciba-Geigy Pharmaceuticals (2002):
Epilepsy
MajorAntipsychotics can lower the seizure threshold and trigger seizures in a dose-dependent manner. Seizures have been reported in patients receiving antipsychotic therapy and may occur in epileptic patients even with maintenance of routine anticonvulsant treatment. Therapy with antipsychotics should be administered cautiously in patients with a history of seizures or other predisposing factors, such as head trauma, CNS abnormalities, and alcoholism. High dosages should be avoided if possible.
7 sources
- Markowitz J, Brown R "Seizures with neuroleptics and antidepressants." Gen Hosp Psychiatry 9 (1987): 135-41
- Lowry MR, Dunner FJ "Seizures during tricyclic therapy." Am J Psychiatry 137 (1980): 1461-2
- "Product Information. Haldol (haloperidol)." McNeil Pharmaceutical (2002):
- "Product Information. Eskalith (lithium)." SmithKline Beecham (2002):
- "Product Information. Moban (molindone)." Gate Pharmaceuticals (2001):
- "Product Information. Orap (pimozide)." Gate Pharmaceuticals
- "Product Information. Loxitane C (loxapine)." Apothecon Inc (2022):
Heart Diseases
MajorLithium should generally not be given to patients with significant cardiovascular disease since the risk of lithium toxicity is high in these patients. Additionally, there have been postmarketing reports of a possible association between lithium therapy and the unmasking of Brugada Syndrome, a disorder characterized by abnormal EKG findings and a risk of sudden death. Lithium should be avoided in patients with this diagnosis or suspicion of it, or that have risk factors, which include unexplained syncope, family history of this syndrome, or family history of unexplained sudden death before the age of 45 years. Therapy with lithium should be administered with extreme caution in patients with preexisting cardiac disease. Consultation with a cardiologist is highly recommended and cardiac monitoring should be completed before and during treatment.
2 sources
- "Product Information. Eskalith (lithium)." SmithKline Beecham (2002):
- "Product Information. Lithobid (lithium)." Ciba-Geigy Pharmaceuticals (2002):
Hypothyroidism
MajorThe use of lithium has been associated with hypothyroidism in 5% to 15% of patient as it blocks the release of thyroxine (T4) and triiodothyronine (T3) mediated by thyrotropin. Therapy with lithium should be administered cautiously in patients with preexisting hypothyroidism. Careful monitoring of the thyroid function is recommended and supplemental thyroid treatment may be required.
2 sources
- "Product Information. Eskalith (lithium)." SmithKline Beecham (2002):
- "Product Information. Lithobid (lithium)." Ciba-Geigy Pharmaceuticals (2002):
Kidney Diseases
MajorLithium is primarily eliminated by the kidneys and should generally not be administered to patients with significant renal dysfunction. Additionally, morphological changes with glomerular and interstitial fibrosis and nephron atrophy have been reported in patients on chronic lithium therapy, although the association has not been clearly established. Kidney function should be assessed in patients prior to starting therapy, during and thereafter and routine urinalysis and renal function tests are recommended. Progressive or sudden changes in renal function indicate the need for reevaluation of treatment. Monitoring lithium serum levels is also recommended.
3 sources
- "Product Information. Eskalith (lithium)." SmithKline Beecham (2002):
- "Product Information. Lithobid (lithium)." Ciba-Geigy Pharmaceuticals (2002):
- Braden GL. Lithium induced renal diseases. In: Greenberg A, ed. "Primer on Kidney Diseases." San Diego, CA: Academic Press Inc. (1994): 173-4
Neuroleptic Malignant Syndrome
MajorNeuroleptic Malignant Syndrome (NMS), a potentially fatal symptom complex, has been reported in association with the use of antipsychotic drugs. The diagnostic evaluation is complicated and the management requires immediate discontinuation of the antipsychotic therapy and intensive symptomatic treatment and medical monitoring. If a patient that has recovered from NMS requires antipsychotic drug treatment again, the reintroduction of therapy should be carefully considered as NMS recurrences have been reported.
5 sources
- "Product Information. Haldol (haloperidol)." McNeil Pharmaceutical (2002):
- "Product Information. Eskalith (lithium)." SmithKline Beecham (2002):
- "Product Information. Moban (molindone)." Gate Pharmaceuticals (2001):
- "Product Information. Orap (pimozide)." Gate Pharmaceuticals
- "Product Information. Adasuve (loxapine)." Teva Pharmaceuticals USA (2015):
Water Intoxication
MajorLithium decreases sodium reabsorption by the renal tubules which could lead to sodium depletion. Therapy with lithium should be administered cautiously in patients with preexisting sodium depletion as the risk of lithium toxicity is increased. Lower dosages may be required. Patients should maintain a normal diet, including salt, and an adequate fluid intake. Monitoring lithium serum concentrations is recommended.
7 sources
- Hurtig DL, Dyson WL "Lithium toxicity enhanced by diuresis." N Engl J Med 290 (1974): 748-9
- Hansen HE, Hestbech J, Olsen S, Amdisen A "Renal function and renal pathology in patients with lithium-induced impairment of renal concentrating ability." Dial Transplant Nephrol 14 (1977): 518-27
- Reisberg B, Gershon S "Side effects associated with lithium therapy." Arch Gen Psychiatry 36 (1979): 879-87
- Depner TA "Nephrotic syndrome secondary to lithium therapy." Nephron 30 (1982): 286-9
- Wood IK, Parmalee DX, Foreman JW "Lithium-induced nephrotic syndrome." Am J Psychiatry 146 (1989): 84-7
- "Product Information. Eskalith (lithium)." SmithKline Beecham (2002):
- "Product Information. Lithobid (lithium)." Ciba-Geigy Pharmaceuticals (2002):
Fever
ModeratePatients with fever may have a lower tolerance to lithium due to increased fluid and sodium loss. Lithium dosage may need to be reduced or suspended in such patients. Monitoring lithium serum levels is recommended.
2 sources
- "Product Information. Eskalith (lithium)." SmithKline Beecham (2002):
- "Product Information. Lithobid (lithium)." Ciba-Geigy Pharmaceuticals (2002):
Hyperprolactinemia
ModerateAntipsychotic drugs can elevate serum prolactin concentrations, and this elevation persists during chronic administration. This should be considered if therapy will be prescribed in patients with previously detected breast cancer as one-third of human breast cancers are prolactin-dependent in vitro. Associated disturbances such as galactorrhea, amenorrhea, gynecomastia, and impotence have been reported. Appropriate laboratory testing and follow-up is advised.
5 sources
- "Product Information. Haldol (haloperidol)." McNeil Pharmaceutical (2002):
- "Product Information. Eskalith (lithium)." SmithKline Beecham (2002):
- "Product Information. Moban (molindone)." Gate Pharmaceuticals (2001):
- "Product Information. Orap (pimozide)." Gate Pharmaceuticals
- "Product Information. Adasuve (loxapine)." Teva Pharmaceuticals USA (2015):
Neutropenia
ModerateThe use of antipsychotics has been associated with events of leukopenia, neutropenia and agranulocytosis. Possible risk factors include preexisting low white blood cell count, and history of drug induced leukopenia/neutropenia. Patients with these risk factors should have complete blood count monitored frequently during the first few months of therapy. Patients should also be monitored for any signs or symptoms of infection. Treatment should be discontinued in any patient who develops a sore throat, fever, stomatitis, or other signs of infection along with a low WBC count or severe neutropenia (ANC < 1000/mm3).
5 sources
- "Product Information. Haldol (haloperidol)." McNeil Pharmaceutical (2002):
- "Product Information. Eskalith (lithium)." SmithKline Beecham (2002):
- "Product Information. Moban (molindone)." Gate Pharmaceuticals (2001):
- "Product Information. Orap (pimozide)." Gate Pharmaceuticals
- "Product Information. Adasuve (loxapine)." Teva Pharmaceuticals USA (2015):