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Lithopik 400mg Tablet SR

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Prescription Required

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Aarpik Pharmaceuticals Pvt Ltd

Salt Composition

Lithium carbonate (400mg)

Overview Lithopik 400mg Tablet SR

For adult patients, Lithopik 400mg Extended-Release tablets effectively manage bipolar disorder and manic episodes. This medication may also be prescribed for certain other behavioral conditions, lessening both the frequency and severity of manic episodes. Administer Lithopik 400mg ER with food, consistently at the same time daily for optimal blood levels. Complete the prescribed course of treatment; missed doses should be taken immediately upon recall. Discontinuation should only occur under medical supervision due to potential adverse effects. Possible side effects encompass tremor, dysarthria, ataxia, nausea, emesis, acne, leukocytosis, and cognitive impairment. Additionally, alopecia, thyroid enlargement, dermatological reactions, and polydipsia may occur. Weight gain is a potential consequence, mitigable through dietary adjustments and physical activity. Long-term use necessitates regular monitoring of thyroid and renal function.

Uses of Lithopik 400mg Tablet SR

Elevated mood states | Bipolar affective disorder

Major Benefits of Lithopik 400mg Tablet SR:

Follow your doctor's instructions precisely regarding dosage and treatment length for this medication. Ingest the 400mg Lithopik SR tablet whole; avoid chewing, crushing, or breaking it. Administer this medication with a meal.

Common Side effects of Lithopik 400mg Tablet SR:

  • Tremors
  • Slurred speech
  • Uncoordinated body movements
  • Nausea
  • Acne
  • Increased white blood cell count
  • Memory impairment
  • Hair loss
  • Goiter (enlarged thyroid gland)
  • Skin rash
  • Increased thirst
  • Weight gain
  • Polyuria
  • Diarrhea
  • Vomiting

How to use Lithopik 400mg Tablet SR:

Consume this medication precisely as prescribed by your physician, adhering to both the dosage and treatment length. Ingest the tablet whole; avoid chewing, crushing, or fracturing it. The Lithopik 400mg Extended-Release tablet should be administered with a meal.

How Lithopik 400mg Tablet SR works:

Lithopik 400mg sustained-release tablets reduce overactive brain nerve cell signaling.

SAFETY ADVICE

AlcoholAlcoholUNSAFE

Combining Lithopik 400mg SR tablets with alcohol is inadvisable.

PregnancyPregnancyCONSULT YOUR DOCTOR

Extended-release Lithopik 400mg tablets pose a confirmed risk to a developing fetus and should not be taken during pregnancy. In exceptional, life-threatening circumstances, a physician might prescribe it if the potential benefits outweigh the known hazards. Physician consultation is essential.

Breast feedingBreast feedingCONSULT YOUR DOCTOR

The extended-release Lithopik 400mg tablet is likely unsafe for breastfeeding mothers. Available human data indicates potential transfer to breast milk, posing a risk to the infant.

DrivingDrivingUNSAFE

Driving ability may be impaired by the use of Lithopik 400mg sustained-release tablets, which can produce adverse effects.

KidneyKidneyCAUTION

Patients with kidney impairment should exercise caution when using Lithopik 400mg sustained-release tablets. Dosage modification of Lithopik 400mg sustained-release tablets may be necessary. Physician consultation is recommended.

LiverLiverSAFE IF PRESCRIBED

The use of Lithopik 400mg sustained-release tablets in individuals with hepatic impairment is likely safe. Existing evidence indicates dose modification may be unnecessary; however, physician consultation is recommended.

What if you forget to take Lithopik 400mg Tablet SR :

Omit any missed Lithopik 400mg SR tablet and resume your usual dosing regimen. Avoid taking a double dose.

Facts to Know About Lithopik 400mg Tablet SR

LabelValue
Type of Compound Naturally Occurring Carboxylic Acids
Addictive None.
Medication Classification Nervous system medications

FAQs on Lithopik 400mg Tablet SR

Noticeable symptom relief from Lithopik 400mg Tablet SR may not be immediate. While individual responses differ, experiencing the full effects can take one to three weeks, or even longer. Do not discontinue Lithopik 400mg Tablet SR without first consulting your physician if you perceive a lack of improvement.
Lithopik 400mg sustained-release tablets may induce neurological effects including drowsiness, vertigo, and cognitive impairment. Visual disturbances such as nystagmus, blurred vision, or scotomas are also possible. Seek medical advice if any such side effects occur. Operation of vehicles or complex equipment should be avoided due to potential risks.
Lithopik 400mg SR tablets can induce kidney dysfunction. Patients with pre-existing severe kidney impairment should not receive this medication. Kidney damage from Lithopik 400mg SR tablets may be irreversible, manifesting as edema, polyuria, and excessive thirst. Prior to commencing Lithopik 400mg SR therapy, your physician will conduct blood tests to assess kidney function. During treatment, any alteration in renal function, whether gradual or abrupt, warrants reassessment of the treatment plan, even if values remain within the normal range.
Taking Lithopik 400mg SR tablets may lead to changes in body weight, either increase or decrease. Monitor your weight while using this medication. Significant weight fluctuations—either gain or loss—warrant a consultation with your physician to determine the cause.
Treatment with Lithopik 400mg sustained-release tablets should commence only where adequate blood level monitoring is possible. This is crucial because Lithopik 400mg sustained-release tablet toxicity is linked to elevated blood concentrations, even at therapeutically effective doses. Consequently, your physician might monitor your blood levels weekly until stable, then weekly for a month, and subsequently monthly.
Follow your doctor's instructions precisely when using Lithopik 400mg Tablet SR. Clarify any uncertainties with your physician. This medication is for oral consumption and may be taken with or without food. Consult your doctor before making significant dietary alterations. Substantial changes in fluid intake or dietary sodium could necessitate increased monitoring of Lithopik 400mg Tablet SR levels.
Prior to commencing Lithopik 400mg Tablet SR, disclose all current medications to your physician. Numerous drugs can interact adversely with Lithopik 400mg Tablet SR. Several medications reduce Lithopik 400mg Tablet SR blood concentrations, impairing efficacy. This includes theophylline (for asthma), caffeine, sodium bicarbonate-containing products, carbonic anhydrase inhibitor diuretics ("water pills"), and urea-based topical treatments.
Lithopik 400mg Tablet SR
20
MRP 24
16% off