Resadol Tablet 325mg+37.5mg

Description

PRESENTATION

Resadol Tablet: Each film coated tablet contains Paracetamol BP 325 mg & Tramadol hydrochloride BP 37.5 mg.

DESCRIPTION

Paracetamol is a non-opiate, non-salicylate analgesic. Tramadol is a centrally acting synthetic opioid analgesic. Although its

mode of action is not completely understood, from animal tests, at least two complementary mechanisms appear applicable: binding

of parent and M1 metabolite to m-opioid receptors and weak inhibition of reuptake of nor-epinephrine and serotonin.

Opioid activity is due to both low affinity binding of the parent compound and higher affinity binding of the O-demethylated

metabolite M1 to m-opioid receptors.

As some other opioid analgesics, Tramadol has been shown to inhibit reuptake of nor-epinephrine and serotonin in vitro. These

mechanisms may contribute independently to the overall analgesic profile of Tramadol.

INDICATIONS

Resadol tablet is indicated for the management of moderate to moderately severe pain in adults.

Resadol tablet is also indicated for the short-term (five days or less) management of acute pain.

DOSAGE & ADMINISTRATION

Resadol tablet can be administered without regard to food.

For the management of moderate to moderately severe pain, the recommended dose is 1 or 2 tablets every 4 to 6 hours as needed for

pain relief up to a maximum of 8 tablets per day.

In case of short-term (five days or less) management of acute pain, the recommended dose is 2 tablets every 4 to 6 hours as needed

for pain relief up to a maximum of 8 tablets per day.

Pediatric & geriatric use: The safety and effectiveness of this combination preparation has not been studied in the pediatric

population. In general, dose selection for an elderly patient should be cautious, reflecting the greater frequency of decreased

hepatic, renal or cardiac function; of concomitant disease and multiple drug therapy.

Use in renal disease: This combination preparation has not been studied in patients with impaired renal function. In patients with

creatinine clearances of less than 30 ml/min, it is recommended that the dosing interval of this combination preparation be

increased but not to exceed 2 tablets every 12 hours.

Use in hepatic disease: This combination preparation has not been studied in patients with impaired hepatic function. The use of

this combination preparation in patients with hepatic impairment is not recommended.

SIDE EFFECTS

The following adverse reactions may happen to this therapy: asthenia, fatigue, hot flushes, dizziness, headache, tremor, abdominal

pain, constipation, diarrhea, dyspepsia, dry mouth, nausea, vomiting, anorexia, anxiety, confusion, euphoria, insomnia,

nervousness, somnolence pruritus, rash, increased sweating etc.

PRECAUTIONS

This combination preparation may impair mental or physical abilities required for the performance of potentially hazardous tasks

such as driving a car or operating machinery.

This combination preparation should not be taken with alcohol containing beverages.

The patient should be instructed not to take this combination preparation in combination with other Tramadol or

Paracetamol-containing products, including over-the-counter preparations.

This combination preparation should be used with caution when taking medications such as tranquilizers, hypnotics or other opiate

containing analgesics.

USE IN PREGNANCY & LACTATION

Pregnancy Category C

There are no adequate and well-controlled studies in pregnant women. This combination preparation should be used during pregnancy

only if the potential benefit justifies the potential risk to the fetus.

This combination preparation is not recommended for obstetrical preoperative medication or for post-delivery analgesia in nursing

mothers because its safety in infants and newborns has not been studied.

STORAGE

Store in cool and dry place. Do not freeze.

COMMERCIAL PACK

Resadol Tablet: Each commercial box contains 3 alu-pvdc blister strips of 10 tablets.