Inhouse product
Indications
Napa
is indicated for fever, common cold and influenza, headache, toothache,
earache, bodyache, myalgia, neuralgia, dysmenorrhoea, sprains, colic pain, back
pain, post-operative pain, postpartum pain, inflammatory pain and post
vaccination pain in children. It is also indicated for rheumatic &
osteoarthritic pain and stiffness of joints.
* রেজিস্টার্ড চিকিৎসকের পরামর্শ মোতাবেক ঔষধ সেবন করুন'
Pharmacology
Paracetamol
exhibits analgesic action by peripheral blockage of pain impulse generation. It
produces antipyresis by inhibiting the hypothalamic heat-regulating centre. Its
weak anti-inflammatory activity is related to inhibition of prostaglandin
synthesis in the CNS.
Paracetamol (Acetaminophen) is thought to act primarily in the CNS, increasing
the pain threshold by inhibiting both isoforms of cyclooxygenase, COX-1, COX-2,
and COX-3 enzymes involved in prostaglandin (PG) synthesis. Unlike NSAIDs,
acetaminophen does not inhibit cyclooxygenase in peripheral tissues and, thus,
has no peripheral anti-inflammatory affects. While aspirin acts as an
irreversible inhibitor of COX and directly blocks the enzyme's active site,
studies have found that acetaminophen indirectly blocks COX, and that this
blockade is ineffective in the presence of peroxides. This might explain why
acetaminophen is effective in the central nervous system and in endothelial
cells but not in platelets and immune cells which have high levels of
peroxides. Studies also report data suggesting that acetaminophen selectively
blocks a variant of the COX enzyme that is different from the known variants
COX-1 and COX-2. This enzyme is now referred to as COX-3. Its exact mechanism
of action is still poorly understood, but future research may provide further
insight into how it works. The antipyretic properties of acetaminophen are
likely due to direct effects on the heat-regulating centres of the hypothalamus
resulting in peripheral vasodilation, sweating and hence heat
Dosage &
Administration
Tablet:
Extended Release Tablet:
Syrup/Suspension:
Suppository:
Paediatric Drop:
Tablet with actizorb technology: It dissolves up to
five times faster than standard Paracetamol tablets. It is a fast acting and
safe analgesic with marked antipyretic property. It is specially suitable for
patients who, for any reason, can not tolerate aspirin or other analgesics.
IV Infusion:
* রেজিস্টার্ড চিকিৎসকের পরামর্শ মোতাবেক ঔষধ সেবন করুন'
Interaction
Patients
who have taken barbiturates, tricyclic antidepressants and alcohol may show
diminished ability to metabolise large doses of Napa. Alcohol can increase the
hepatotoxicity of Napa overdosage. Chronic ingestion of anticonvulsants or oral
steroid contraceptives induce liver enzymes and may prevent attainment of
therapeutic Napa levels by increasing first-pass metabolism or clearance.
Contraindications
It
is contraindicated in known hypersensitivity to Paracetamol.
Side Effects
Side
effects of Napa are usually mild, though haematological reactions including
thrombocytopenia, leucopenia, pancytopenia, neutropenia, and agranulocytosis
have been reported. Pancreatitis, skin rashes, and other allergic reactions
occur occasionally.
Pregnancy &
Lactation
Epidemiological
studies in human pregnancy have shown no ill effects due to Paracetamol used in
the recommended dosage, but patients should follow the advice of their doctor
regarding its use. Paracetamol is excreted in breast milk, but not in a
clinically significant amount. Available published data do not contraindicate
breast feeding.
Precautions &
Warnings
Care
is advised in the administration of Napa to patients with severe renal or
severe hepatic impairment. The hazard of overdose is greater in those with
non-cirrhotic alcoholic liver disease. Do not exceed the stated dose. Patients
should be advised not to take other Napa-containing products concurrently. Napa
should only be used by the patient for whom it is prescribed when clearly
necessary.
Administration of Napa in doses higher than recommended may result in hepatic
injury, including the risk of severe hepatotoxicity and death. Do not exceed
the maximum recommended daily dose of Napa. Use caution when administering Napa
in patients with the following conditions: hepatic impairment or active hepatic
disease, alcoholism, chronic malnutrition, severe hypovolemia (e.g., due to
dehydration or blood loss), or severe renal impairment (creatinine clearance
< 30 ml/min). There were infrequent reports of life-threatening anaphylaxis
requiring emergent medical attention. Discontinue Napa IV immediately if
symptoms associated with allergy or hypersensitivity occurs. Do not use Napa IV
in patients with Napa allergy.
Use in Special
Populations
Pediatric Use: The safety and effectiveness of Napa IV for
the treatment of acute pain and fever in pediatric patients ages 2 years and
older is supported by evidence from adequate and well-controlled studies of
Napa IV in adults.
Geriatric
use: No overall differences in safety or effectiveness were
observed between these subjects and younger subjects, and other reported
clinical experience has not identified differences in responses between the
elderly and younger patients.
Patients
with Hepatic Impairment: Napa is contraindicated in patients with severe hepatic
impairment or severe active liver disease and should be used with caution in
patients with hepatic impairment or active liver disease. A reduced total daily
dose of Napa may be warranted.
Patients
with Renal Impairment: In cases of severe renal impairment (creatinine clearance <
30 ml/min), longer dosing intervals and a reduced total daily dose of Napa may
be warranted.
Overdose Effects
Liver
damage is possible in adults who have taken 10 g or more of Napa. Ingestion of
5 g or more of Napa may lead to liver damage if the patient has following risk
factors: If the patient is on long term treatment with Carbamazepine,
Phenobarbitone, Phenytoin, Primidone, Rifampicin, St John’s Wort or other drugs
that induce liver enzymes, or regularly consumes Ethanol in excess of
recommended amounts, or is likely to be Glutathione deplete e.g. eating
disorders, cystic fibrosis, HIV infection, starvation, cachexia.
Symptoms: Symptoms of Napa
overdose in the first 24 hours are pallor, nausea, vomiting, anorexia and
abdominal pain. Liver damage may become apparent 12 to 48 hours after
ingestion. Abnormalities of glucose metabolism and metabolic acidosis may
occur. In severe poisoning, hepatic failure may progress to encephalopathy,
haemorrhage, hypoglycaemia, cerebral oedema and death. Acute renal failure with
acute tubular necrosis, strongly suggested by loin pain, haematuria and
proteinuria, may develop even in the absence of severe liver damage. Cardiac
arrhythmias and pancreatitis have been reported. Immediate treatment is
essential in the management of Napa overdose. Treatment with activated charcoal
should be considered if the overdose has been taken within 1 hour. Plasma Napa
concentration should be measured at 4 hours or later after ingestion (earlier
concentrations are unreliable). Treatment with N-acetylcysteine may be used up
to 24 hours after ingestion of Napa. However, the maximum protective effect is
obtained up to 8 hours post-ingestion. The effectiveness of the antidote
declines sharply after this time. If required the patient should be given
intravenous N-acetylcysteine, in line with the established dosage schedule. If
vomiting is not a problem, oral Methionine may be a suitable alternative for
remote areas, outside hospital. Management of patients who present with serious
hepatic dysfunction beyond 24 hours from ingestion should be discussed with the
NPIS or a liver unit.
Therapeutic Class
Non
opioid analgesics
Storage Conditions
Keep
in a dry place away from light and heat. Keep out of the reach of children.
Common Questions about
Napa 500 mg Tablet
What is Napa 500 mg Tablet?
Napa 500 mg Tablet is
a medication that performs its action by obstructing the release of pain and
fever chemical messengers.
What are the uses of Napa 500 mg Tablet?
Napa 500 mg Tablet is
used for the treatment and prevention of conditions and symptoms of diseases
like Post immunization pyrexia, menstrual cramps and fever.
What are the Side Effects of Napa 500 mg Tablet Napa 500 mg
Tablet?
Allergic reaction,
gastric ulcers, fatigue, anemia, nausea and vomiting are possible side effects.
What are the instructions for storage and disposal Napa 500 mg
Tablet?
Napa 500 mg Tablet
should be stored at room temperature, away from heat and direct light. Keep it
away from the reach of children and pets.
Should I use Napa 500 mg Tablet empty stomach, before food or after
food?
If you take Napa 500
mg Tablet with the food, the reactions that took place in the body carry-outs
in a much effective manner.
How long do I need to use Napa 500 mg Tablet before I see
improvement in my conditions?
Napa 500 mg Tablet
should be consumed, until the complete eradication of the disease. It is
advised to use, till the time directed by your doctor.
Is there any food or drink I need to avoid while taking Napa 500
mg Tablet?
You can follow your
normal diet under the usage of Napa 500 mg Tablet.
Will Napa 500 mg Tablet be more effective if taken in more than
the recommended dose?
There is no need to
take Napa 500 mg Tablet more than its recommended doses.
Can I take other medications along with Napa 500 mg Tablet?
Do not use any OTC for
cough, cold, allergy, or pain medication without consulting your doctor or
pharmacist. Napa 500 mg Tablet contains many combination of medicines. If you
use certain products together you may accidentally use too much of Napa 500 mg
Tablet.
Can I take Napa 500 mg Tablet with antibiotics?
There are hundreds of
antibiotics used to treat infections, so once you receive your prescription,
ask your doctor or pharmacist if you can also take Napa 500 mg Tablet at
the same time that you take the antibiotic.
Is Napa 500 mg Tablet an NSAID drug?
No, Napa 500 mg Tablet
is not classified as an NSAID (nonsteroidal anti-inflammatory drug). It is
classified as a miscellaneous analgesic for mild to moderate pain and fever.
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