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Nordeplin-PM Tablet SR

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Prescription Required

Marketer

Archicare Limited

Salt Composition

Pregabalin (75mg) + Nortriptyline (10mg) + Methylcobalamin (1500mcg)

Overview Nordeplin-PM Tablet SR

Nordeplin-PM SR tablets combine medications to manage neuropathic pain. Their mechanism involves modulating nerve cell calcium channel activity, thereby reducing pain signals. Simultaneously, they boost brain neurotransmitters crucial for mood regulation and nerve protection. Nordeplin-PM SR can be ingested with or without food, but consistent daily timing ensures stable drug levels. Always follow your physician's prescribed dosage and duration. Missed doses should be taken immediately upon recall. Complete the entire treatment regimen, regardless of symptom improvement. Abrupt cessation may exacerbate symptoms. Common side effects include constipation, weight gain, and dry mouth. Dizziness and drowsiness are possible; avoid driving or mentally demanding tasks until effects are known. Weight gain may occur; a balanced diet and regular exercise are recommended. Report any unusual mood or behavioral shifts, new or worsening depression, or suicidal ideation to your doctor. Disclose any kidney or liver conditions, and list all other medications you are using, as interactions may affect Nordeplin-PM SR's efficacy. Inform your doctor if you are pregnant, planning pregnancy, or breastfeeding.

Primary Ingredients of Nordeplin-PM Tablet SR

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Uses of Nordeplin-PM Tablet SR

Managing neuropathic pain

Major Benefits of Nordeplin-PM Tablet SR:

Follow your doctor's instructions precisely regarding dosage and treatment length for this medication. Ingest the tablet whole; avoid chewing, crushing, or breaking it. Nordeplin-PM Tablet SR can be taken with or without food, however, consistency in timing is recommended.

Common Side effects of Nordeplin-PM Tablet SR:

  • Orthostatic hypotension (sudden lowering of blood pressure on standing)
  • Increased heart rate
  • Difficulty in urination
  • Decreased appetite
  • Nausea
  • Vomiting
  • Constipation
  • Weight gain
  • Dizziness
  • Sleepiness
  • Tiredness
  • Blurred vision
  • Dryness in mouth
  • Uncoordinated body movements
  • Diarrhea
  • Headache

How to use Nordeplin-PM Tablet SR:

Follow your doctor's instructions precisely regarding the dosage and treatment length for this medication. The tablet should be swallowed whole; avoid chewing, crushing, or breaking it. Nordeplin-PM SR Tablets can be administered with or without food, however, consistent timing is recommended.

How Nordeplin-PM Tablet SR works:

Nordeplin-PM SR tablets contain pregabalin, nortriptyline, and methylcobalamin, working synergistically to alleviate neuropathic pain. Pregabalin, an alpha-2-delta calcium channel modulator, reduces pain transmission at the nerve cell level. Nortriptyline, a tricyclic antidepressant, elevates serotonin and noradrenaline, neurotransmitters that inhibit pain signal propagation in the brain. Methylcobalamin, a vitamin B12 derivative, supports myelin sheath production and repair, protecting and restoring nerve fiber health. This combined action effectively targets neuropathic pain.

SAFETY ADVICE

AlcoholAlcoholUNSAFE

Taking Nordeplin-PM extended-release tablets with alcohol can lead to significant sleepiness.

PregnancyPregnancyCONSULT YOUR DOCTOR

Taking Nordeplin-PM SR tablets during pregnancy may pose risks. While human research is scant, animal studies indicate potential harm to a developing fetus. A physician will assess the advantages against possible dangers prior to prescribing. Seek medical advice.

Breast feedingBreast feedingCONSULT YOUR DOCTOR

The extended-release Nordeplin-PM tablet likely poses a risk during lactation. Scant evidence from human studies indicates potential transfer to breast milk, with consequent infant harm.

DrivingDrivingUNSAFE

Driving ability may be impaired by Nordeplin-PM Tablet SR, due to potential side effects that can reduce alertness.

KidneyKidneyCAUTION

Patients with kidney impairment should use Nordeplin-PM Tablet SR cautiously, as dosage modification may be necessary. Physician consultation is advised.

LiverLiverSAFE IF PRESCRIBED

The use of Nordeplin-PM Tablet SR in patients with hepatic impairment is likely safe. Available evidence indicates dose modification may be unnecessary; however, physician consultation is recommended.

What if you forget to take Nordeplin-PM Tablet SR :

Should you forget a Nordeplin-PM Tablet SR dose, administer it promptly. However, if your next scheduled dose is imminent, omit the missed dose and resume your usual dosing regimen. Avoid taking a double dose.

Facts to Know About Nordeplin-PM Tablet SR

LabelValue
Potential for Dependence None.
Treatment Category Nervous system medications

FAQs on Nordeplin-PM Tablet SR

Gabapentin, nortriptyline, and methylcobalamin are combined in Nordeplin-PM SR tablets. This formulation treats neuropathic pain by modulating the activity of damaged or overly sensitive nerves within the brain, thus reducing pain perception. Furthermore, it supports the repair of nerve tissue.
Discontinuing Nordeplin-PM Tablet SR prematurely, even with pain relief, is inadvisable. Follow your physician's prescribed regimen. Abrupt cessation may trigger withdrawal effects including anxiety, insomnia, nausea, pain recurrence, and diaphoresis. A gradual dose reduction is recommended prior to complete discontinuation.
Taking Nordeplin-PM Tablet SR may increase appetite, potentially leading to weight gain. Weight management is simpler than weight loss. Maintain a balanced diet without enlarging portions. Limit high-calorie foods like sugary drinks, fried foods, processed snacks, and desserts. Between meals, opt for fruits, vegetables, and low-calorie choices instead of unhealthy snacks. Regular physical activity aids in preventing weight gain. Consistent healthy eating and exercise may prevent any weight increase.
Nordeplin-PM Tablet SR can induce drowsiness or cause sudden sleep onset during routine tasks. These episodes may occur without prior warning signs like drowsiness. Refrain from operating vehicles, machinery, working at heights, or engaging in hazardous activities initially, until the medication's effects are understood. Report any such incidents to your physician during treatment.
Nordeplin-PM Tablet SR may impact sexual function in both genders. Reduced libido, erectile difficulties (inability to achieve or sustain an erection), and anorgasmia are frequently reported. Decreased sexual satisfaction and discomfort during intercourse may also occur. Consult your physician if these issues arise, but do not discontinue Nordeplin-PM Tablet SR without medical advice.
Uncommon and infrequent adverse reactions associated with Nordeplin-PM Tablet SR include: altered body temperature, respiratory distress, rapid heartbeat (palpitations), muscular weakness, gait instability, impaired motor coordination or slowed reflexes, atypical mood or behavioral shifts (e.g., agitation, anxiety, or euphoria), depressive symptoms, hallucinations, illogical thought processes, visual disturbances (blurred or double vision), involuntary eye movements (nystagmus), visual impairment, and indicators of recurrent infections like pyrexia, intense chills, pharyngitis, or oral ulcers. While infrequent, these reactions warrant immediate medical evaluation due to their potential severity.
Patients may notice some improvement with Nordeplin-PM Tablet SR within two weeks. Complete therapeutic effects, however, typically manifest after two to three months, or possibly longer.
Should you miss a scheduled dose of Nordeplin-PM Tablet SR, and your next dose is imminent, omit the missed dose and continue with your regular dosing schedule. If, however, sufficient time remains before your next dose, take the missed dose immediately and then resume your usual medication regimen. Avoid doubling up on doses to compensate for a missed one; doing so might heighten the chance of adverse effects. For any uncertainty regarding missed doses, seek guidance from your healthcare provider.
If this occurs, promptly contact your physician or proceed to the closest emergency room for assessment. This is advised regardless of the presence or absence of symptoms. Immediate medical care may be necessary. Overdose symptoms can manifest as lethargy, fatigue, gait instability, diplopia, dysarthria, diarrhea, disorientation, blurred vision, vertigo, fluctuating body temperature, respiratory distress, and tachycardia.
Increasing your medication dosage beyond the prescribed amount won't necessarily improve its effectiveness; instead, it could heighten the risk of severe adverse reactions and poisoning. Should your symptoms worsen despite adhering to the recommended dosage, seek medical advice for reassessment.
Taking Nordeplin-PM Tablet SR may affect cognitive function and reflexes. Exercise caution when operating machinery or engaging in activities demanding alertness. Alcohol consumption should be avoided during Nordeplin-PM Tablet SR treatment as it can potentiate the drug's effects, posing a safety risk. Grapefruit and its juice may interact negatively with this medication, potentially leading to adverse reactions. Minimize sun exposure and the use of tanning beds. Nordeplin-PM Tablet SR increases sun sensitivity; wear protective clothing and sunscreen when outside during daylight hours.
Regular monitoring by your physician is recommended following commencement of Nordeplin-PM Tablet SR therapy. Consult your doctor immediately if your symptoms persist despite adherence to the prescribed Nordeplin-PM Tablet SR dosage, or if any adverse effects significantly impact your daily life.
Retain your medication within its original packaging until needed. Store the tablets in a cool, dry location. Keep them out of the reach and view of children. Proper disposal of any remaining medication is essential to prevent accidental ingestion by children, pets, or others.
Nordeplin-PM Tablet SR has an expiration date. Confirm the expiration date printed on the product packaging. Discard Nordeplin-PM Tablet SR after this date.
Nordeplin-PM Tablet SR
139
MRP 169
17% off