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Store this medication in a non-threatening room to prevent theft, abuse, or misuse. If someone accidentally swallows this product, seek medical assistance immediately.
Norco 5-325
Norco 5/325 (hydrocodonacetaminophen and bitartrate) is considered an opioid analgesic and anti-rock um (cough suppressant) combined with fever and anesthetic and is used to treat from moderate to fairly severe pain. norco 5/325 is available as a joint medicine Norco 5/325 can be used as a joint medicine.
What are the side effects of Norco 5/325?
Common side effects of Norco 5/325 include
- Udder,
- Nausea,
- Vomiting and diarrhea,
- Constipation,
- stomach complaints,
- Dizziness or drowsiness,
- Restlessness,
- headache,
- Mood swings
- blurred vision,
- Whistles, or
- dry mouth.
Description.
Norco® (bitartrate and hydrocodone acetaminophen) is administered in tablet form for oral administration.
Hydrocodone bitartrate is considered an opioid analgesic and anti-invisible and is found in the form of elegant snow white crystals or crystal powder. It affects light. Its chemical name is 4, 5α-epoxy-3-methoxy-17-methylmorphine-6-one Tartrate (1:1) Hydlate (2:5). The appropriate structural formula includes.
Acetaminophen, 4 feet of hydroxyacetani, a slightly bitter, broken white, tasteless crystalline powder, supplies an atypical, non-salicylic acid analgesic and anti-fat. It contains the appropriate structural formula.
Norco® for oral administration is available in appropriate potent aspects.
Hydrocodone
acetaminophen bitartrate
Norco®7, 5/325 7, 5 mg 325 mgNorco®10/32510 mg 325 mg
In addition, each tablet has an appropriate inactive ingredient. Cross amelia, crosvidone, magnesium stearate, microcrystalline cellulose, povidone, and stearic acid from Pretil. 7, 5 mg/325 mg tablets contain aluminum; C, 10 mg/325 mg tablets have a yellowish d& amp; C #10; and C#10. Complies with USP 1 solubility test.
Indications and Dosage
Indications
Norco® is indicated for lighting from moderate to equally severe pain
Medication and Administration
Dosage should be adjusted to the severity of the pain and the patient’s response. Nevertheless, it should be noted that tolerance to hydrocodone may develop with later use and the frequency of less favorable effects is dose-related.
The usual dosage for adults is one pill every 4 to 6 hours, depending on need for pain. Total daily dosage may not exceed 6 pills.
How supplied.
Norco®7. 5/325 is available as an orange pill in capsule form on one side and unmasked with “Norco®729” on the other. Each pill contains 7, 5 mg of Vitalotonate and 325 mg of Acetaminophen. They are delivered in the following manner
500 bottles of 100 bottles of 100 bottles of 30 bottles of 30
Norco 10/325 is available as yellowish pills in capsule form with “Norco 539” mentioned on one side and “Norco 539” on the other. Each pill contains 10 mg of hydrocodone bitartrate and 325 mg of acetaminophen. They are delivered in the following ways
100 bottles of 500
Store at 20°-25°C (68°-77°F). [See USP Control Room Heat].
Distribute in sturdy, child-resistant packaging with child closure.
Watson Pharma, Inc. a subsidiary of Watson, Pharmaceuticals, Inc, Corona, CA 92880 USA 14716. Reviewed July 2007, Cardinal Health, Zanesville, OH 43701.
Side Effects and Interactions Between Medications
Side Effects
The most reported side effects are lightheadedness, dizziness, sedation, drowsiness, and nausea. These side effects seem to occur more in outpatients than in sprayed patients, and some of these side effects are more likely to be illuminated if the patient does not get worse.
Other side effects are.
CNS: Fractionation, intellectual bonding, lethargy, failure of intellectual and physiological performance, agitation, fear, abnormality, psychological sensitivity, mood composition.
Gastrointestinal system: prolonged administration of Norco® may lead to constipation.
Muscular system: ureteral spasms, premenstrual cramping spasms, and opiate-induced urine retention.
Respiratory depression. Hydrocodone bitatrate may lead to dose-related respiratory depression by working specifically on the respiratory centers of the brainstem (see overdose).
Special sensitivities: cases of hearing loss or permanent loss. Usually reported in patients who have obtained an overdose.
Dermatology: skin rash, itching.
Possible effects of acetaminophen include allergic reactions, rashes, thrombocytopenia, agranulocytosis, and other unwanted events related to the way the product is manufactured. Possible consequences from the highest doses are listed in the PEREDOSAGE section.
Drug Abuse and Dependence
Controlled Substances
NORCO® is classified as a Schedule III controlled substance.
Abuse and Dependence
Repeated use of the drug may result in psychological bondage, physical bondage, and tolerance. Therefore, this product should be used with caution. However, short-term use of NORCO® for the treatment of pain is unlikely to result in psychological dependence.
Physical dependence, a situation in which prolonged use of the product is necessary to avoid withdrawal syndromes, becomes clinically significant only after several months of continuous drug use, while physiological dependence of a less severe degree may occur after only a few uses. Develop daily use. Drug Therapy. Tolerance occurs when increasingly higher doses are required to achieve the same degree of analgesia, first by reducing the duration of analgesic effect and then by reducing the intensity of analgesia. The degree of tolerance varies from patient to patient.
Drug Interactions
Additive CNS depression may be observed in patients receiving other medications, antihistamines, neuroleptics, sedatives, or other CNS depressants (including alcohol) with NORCO® products. If combination therapy is considered, the dose of one or both drugs should be reduced.
Concomitant use of MAOIs or tricyclic antidepressants with hydrocodone products may enhance the effects of antidepressants or hydrocodone.
Drug Interactions and Laboratory Tests
Acetaminophen may cause false positive test results for 5-hydroxyindoleacetic acid in urine.
Warning.
Respiratory Suppression.
Hydrocodone used at high doses or in sensitive patients may affect the respiratory midpoint of the brainstem and cause dose-dependent respiratory depression. Hydrocodone may still affect the midline, which controls respiratory rhythm, causing irregular and periodic breathing.
Head trauma and excessive intracranial pressure
The drug’s respiratory depressant effect and ability to increase cerebral fluid pressure can become hyperbolic in the presence of head trauma, other intracranial lesions, or an already existing increase in intracranial pressure. In addition, the drug can cause side effects that allow for clinical treatment of patients with head trauma.
Acute abdominal disorders
Administration of the drug may cloud the diagnosis or clinical treatment of patients with acute abdominal disorders.
Precautionary Measures
Preventive Measures
In general
Special Risks to Patients
As with other narcotic analgesics, Norco® should be used with caution in older or weakened patients and in patients with severe liver or renal dysfunction, hypothyroidism, Addison’s disease, prostatic lipidosis or urethral stricture. Normal precautions must be taken into account and the possibility of respiratory depression must be considered.
Cough.
Hydrocodone destroys the cough reflex. As with all medications, caution should be exercised when using Norco® after surgery and in patients with pulmonary disease.
Laboratory Studies
In patients with liver or kidney disease, liver and/or kidney tests should be used to check the effects of treatment.
Carcinogenesis, mutagenesis, birth defects
No adequate animal studies have been conducted to determine whether hydrocodone or acetaminophen may cause carcinogenesis, mutagenesis, or fertility problems.
Pregnancy
Teratogenic Effects
Pregnancy Category c
There are no adequate and fully controlled studies in pregnant women; NORCO® is only used during pregnancy when the potential for fetal risk may be justified.
Non-psychotic effects
Babies of mothers who have used opioids in the family at intervals become physically dependent. Withdrawal symptoms include irritability and excessive nags, vibrations, hyperactive reflexes, exaggerated breathing, more stools, sneezing, yawning, nausea, and fever. The severity of the syndrome does not necessarily correlate with useful time or maternal opioid dose. There is no consensus on the best way to address withdrawal.
Labor and Delivery
As with all medications, administration of this product to the mother may lead to some degree of respiratory depression in the newborn just prior to birth, especially if high doses are used.
Latent mothers.
Acetaminophen is excreted in small amounts in breast milk, but the significance of the effect on the infant is unknown. It is not clear whether hydrocodone in breast milk differs. Almost all drugs are different in breast milk, and because of the potential side effects of hydrocodone and acetaminophen on nursing infants, it is prudent to consider the importance of breastfeeding when deciding whether to discontinue breastfeeding or reduce the drug dose. Products for mothers.
Pediatric use
Safety and efficacy in pediatric patients have not been established.
For use in the elderly
Clinical studies of hydrocodone hydrogen tartrate 5 mg and acetaminophen 500 mg did not include sufficient numbers of subjects 65 years of age or older to determine whether they would respond differently than younger subjects. Other clinical skills reported showed no difference in response between older and younger patients. In general, doses for older patients should be chosen carefully, usually starting at the lower end of the dose spectrum, because of the frequency of liver, kidney, or heart dysfunction and concomitant disease or other pharmacotherapy.
The major metabolites of hydrocodone and acetaminophen are known to be largely differentiated by the kidneys. Therefore, patients with impaired renal function may be at increased risk for toxic reactions due to accumulation of the parent compound and/or metabolites in plasma. Because older patients are more likely to have impaired renal function, it is prudent to exercise caution in dose selection, which may be healthier for renal function prognosis.
Hydrocodone can cause discomfort and infestation in the elderly. Elderly patients should usually start with low-dose hydrocodone tartrate and acetaminophen tablets, which are available with caution.
Overdose and Contraindications
Overdose.
Following an acute overdose, toxicity may occur as with hydrocodone or acetaminophen.
Signs and Symptoms
Hydrocodone
A severe overdose of hydrocodone is characterized by respiratory depression (decreased respiratory rate and/or size, chain-stoke breathing, cyanosis), extreme drowsiness suitable for lake or coma, and leekpotonia. Severe overdose can cause apnea, circulatory arrest, cardiac arrest, and death.
Acetaminophen.
Acetaminophen repair: dozonom, potentially fatal liver necrosis, is considered a slightly irritating side effect. Necrosis of the kidney tubules, hypocondensation com sleep, and thrombocytopenia still have every opportunity to run.
Initial symptoms after a possible hepatotoxic overdose are nausea, vomiting, paralysis, and mal laziness. Clinical and laboratory delivery toxicity certificates may be evident 48 to 72 hours after administration.
In mature individuals, liver poisoning is sometimes reported, with sudden overdose of less than 10 grams or fatal finals at less than 15 grams.
CARE
A single off or repeated overdose with hydrocodone and acetaminophen is considered a potentially fatal overdose polydrug and consultation with a topical anti-GIF center is recommended.
Direct treatment includes cardiopulmonary support and measures to reduce drug absorption. If the patient is alert, nausea should be induced automatically or IPECAC syrups should be used (appropriate pharyngeal and laryngeal reflexes). Oral active carbon (1 g/kg) followed by gastric contents should occur; the first dose should be accompanied by appropriate catharticum. With repeated doses, the cathartics can be integrated into other doses as needed. Hypotension is generally considered a hematologic condition and must be answered with water. Vasopressors and other support measures should be used as prescribed. A cuffed endotracheal tube should be inserted for gastric rinsing of nonresponsive patients and for additional ventilation if needed.
Careful care follows in the footsteps of caution to maintain adequate pulmonary ventilation. In severe cases of poisoning, abdominal dialysis or preferably hemodialysis can be performed. If hypovolemia occurs as a result of acetaminophen overdose, vitamin K should be administered intravenously.
Naloxone, a narcotic antagonist, can reverse depression and com sleep breathing as a result of opioid overdose. 0.4 mg to 2 mg of naloxone hydrochloride is administered to the parent. During periods of hydrocodone exposure that may exceed naloxone, the patient should be kept under constant supervision and, if necessary, repeat doses of antagonists should be administered to maintain adequate respiration.
In the absence of clinically significant respiratory or psychiatric depression, narcotic antagonists need not be administered.
If the acetaminophen dose exceeds 140 mg/kg, acetylcysteine should be administered as soon as possible. Serum acetaminophen values should be obtained as values more than 4 hours after ingestion are helpful in predicting acetaminophen toxicity. Do not wait for acetaminophen test results before initiating therapy. Liver enzymes should be obtained early and repeated at 24-hour intervals.
Memoglobinamia 30%, when administered by slow intravenous infusion, traces of methylene blue cultures.
The mature toxic dose of acetaminophen is 10 g.
Contraindications
Norco® is not indicated for patients who have previously demonstrated hypersensitivity to hydrocodone or acetaminophen.
Patients with known hypersensitivity to other opioids may exhibit cross-sectional effects to hydrocodone.
Clinical Pharmacology
Clinical Pharmacology
Hydrocodone is a semisynthetic narcotic analgesic that has a number of effects very similar to those of codeine. Most of these involve the central nervous system and smooth muscle. The true mechanism of action of hydrocodone and other opiates is unknown, but is believed to involve the presence of opiate receptors in the CNS. In addition to analgesics, narcotics can cause drowsiness, mood swings, and intellectual disability.
The analgesic effects of acetaminophen include peripheral effects, but their specific device has not yet been oriented. Its analgesic potency is mediated by the thermoregulatory centers of the hypothalamus. Acetaminophen inhibits prostaglandin synthase. Therapeutic doses of acetaminophen have little effect on the psychovascular or respiratory systems. However, toxic doses may cause circulatory disturbances and rapid shortness of breath.
Pharmacokinetics
The behavior of the individual components is described below.
Hydrocodone
After 5 adult male subjects received a 10 mg oral dose of hydrocodone, the mean peak concentration was 23.6 ± 5.2 ng/mL. The highest serum level was reached after 1.3 ± 0.3 hours, with a half-life determined at 3.8 ± 0.3 hours. Hydrocodone exhibits a difficult metabolic structure with O-demethylation, N-demethylation, and 6-ketonization to the appropriate 6-α- and 6-β-hydroxy metabolites. See Overdose for toxicity information.
Acetaminophen.
Acetaminophen is quickly absorbed from the gastrointestinal tract and spread to most body tissues. The half-life of plasma varies from 1.25 to 3 hours, but can be prolonged by liver damage and subsequent overdose. Acetaminophen elimination consists primarily of hepatic metabolism (binding) and further renal excretion of metabolites. Approximately 85% of oral doses are seen in the urine within 24 hours of administration, mostly as glucuronide jugat, with a few other conjugates and incessant drugs. For toxicity, see Overdose.
Drug Guide
Patient Information
As with all drugs, hydrocodone may affect the intellectual and/or physiological abilities necessary to perform potentially unsafe tasks, such as driving a motor vehicle or operating machinery. Patients should be warned accordingly.
Alcohol and other CNS depressants, when ingested in support of this combination product, may cause additional CNS depression and should be ignored.
Hydrocodone is addictive. A patient may take the product only as long as it is prescribed, unless otherwise specified, in specified quantities.
He produces the product in specified quantities and for as long as it is prescribed, unless otherwise specified.
lortab 5 m g-325 mg pill – Introduction, side effects, and almost everything else
Hydrocodone/acetaminophen poses a risk of abuse and dependence and can lead to overdose and death. Hydrocodone/acetaminophen can also cause severe and possibly fatal breathing problems. To reduce this risk, your doctor should ask you to take the shortest dose of hydrocodone/acetaminophen that works and to take it as soon as possible. For more information on addiction, see the section
Ask your own doctor or pharmacist if you need naloxone to treat an opioid overdose. Inform your family and housemates about the symptoms of opioid overdose and how to treat them.
Increasing the dose after starting this medication or taking it at the wrong dose/intensity increases the risk of breathing problems. Taking this medication with alcohol or other medications that can cause drowsiness or breathing difficulties can result in serious side effects, including death. Additionally, other medications may affect the removal of hydrocodone/acetaminophen from the body, which could affect the action of hydrocodone/acetaminophen. Be sure to understand how to take hydrocodone/acetaminophen and which other medications should be ignored. Refer to the Drug Interactions section for more information. Seek medical attention immediately if you experience very serious side effects such as slow/short breathing, unusual lightheadedness, drowsiness/ dizziness, difficulty getting up, etc.
Store this medication in a non-threatening room to prevent theft, abuse, or misuse. If someone accidentally swallows this product, seek medical assistance immediately.
Acetaminophen is considered one of the ingredients in this product. Very high doses of acetaminophen can cause serious (possibly fatal) liver disease. Adults should not take more than 4,000 milligrams (4 grams) of acetaminophen per day. People with liver problems and babies should reduce their acetaminophen intake. Ask your doctor or pharmacist how much acetaminophen you can safely take.
Do not use other products containing acetaminophen without consulting your doctor or pharmacist beforehand. Acetaminophen is found in many over-the-counter and prescription medications, including pain relievers, fever reducers, and cough medicines. Check the labels of all medications to see if they contain acetaminophen, and ask your pharmacist if you are unsure.
Seek immediate medical attention if you have taken a large dose of acetaminophen (overdose), even if you feel well. Signs of overdose include nausea, vomiting, loss of appetite, sweating, stomach/abdominal pain, severe fatigue, yellow eyes/skin, and dark urine.
Daily use of alcohol can destroy the liver, especially when combined with acetaminophen. Use caution with alcohol.
Before using this drug, women of fertile age should talk to their doctor about the risks and benefits. Tell your doctor if you are pregnant or want to become pregnant. During pregnancy, this medication may be used only when clearly needed. If used in the direction of the first two months of pregnancy, it may slightly increase the risk of birth defects. Additionally, this use may be harmful to the fetus at prolonged or high doses within the expected delivery date. To minimize risk, take the shortest effective dose possible for the shortest possible time. Children born to mothers who use this product for extended periods of time may develop serious (possibly fatal) withdrawal symptoms. Tell your doctor immediately if you notice any signs with your newborn baby. Sobbing, slow/small breathing, irritability, shaking, nausea, diarrhea, poor or difficult food.
Warning:
Hydrocodone/acetaminophen poses a risk of abuse and dependence and can lead to overdose and death. Hydrocodone/acetaminophen can also cause severe and possibly fatal breathing problems. To reduce this risk, your doctor should ask you to take the shortest dose of hydrocodone/acetaminophen that works and to take it as soon as possible. For more information on addiction, see the section
Ask your own doctor or pharmacist if you need naloxone to treat an opioid overdose. Inform your family and housemates about the symptoms of opioid overdose and how to treat them.
Increasing the dose after starting this medication or taking it at the wrong dose/intensity increases the risk of breathing problems. Taking this medication with alcohol or other medications that can cause drowsiness or breathing difficulties can result in serious side effects, including death. Additionally, other medications may affect the removal of hydrocodone/acetaminophen from the body, which could affect the action of hydrocodone/acetaminophen. Be sure to understand how to take hydrocodone/acetaminophen and which other medications should be ignored. Refer to the Drug Interactions section for more information. Seek medical attention immediately if you experience very serious side effects such as slow/short breathing, unusual lightheadedness, drowsiness/ dizziness, difficulty getting up, etc.
Store this medication in a non-threatening room to prevent theft, abuse, or misuse. If someone accidentally swallows this product, seek medical assistance immediately.
Acetaminophen is considered one of the ingredients in this product. Very high doses of acetaminophen can cause serious (possibly fatal) liver disease. Adults should not take more than 4,000 milligrams (4 grams) of acetaminophen per day. People with liver problems and babies should reduce their acetaminophen intake. Ask your doctor or pharmacist how much acetaminophen you can safely take.
Do not use other products containing acetaminophen without consulting your doctor or pharmacist beforehand. Acetaminophen is found in many over-the-counter and prescription medications, including pain relievers, fever reducers, and cough medicines. Check the labels of all medications to see if they contain acetaminophen, and ask your pharmacist if you are unsure.
Seek immediate medical attention if you have taken a large dose of acetaminophen (overdose), even if you feel well. Signs of overdose include nausea, vomiting, loss of appetite, sweating, stomach/abdominal pain, severe fatigue, yellow eyes/skin, and dark urine.
Daily use of alcohol can destroy the liver, especially when combined with acetaminophen. Use caution with alcohol.
Before using this drug, women of fertile age should talk to their doctor about the risks and benefits. Tell your doctor if you are pregnant or want to become pregnant. During pregnancy, this medication may be used only when clearly needed. If used in the direction of the first two months of pregnancy, it may slightly increase the risk of birth defects. Additionally, this use may be harmful to the fetus at prolonged or high doses within the expected delivery date. To minimize risk, take the shortest effective dose possible for the shortest possible time. Children born to mothers who use this product for extended periods of time may develop serious (possibly fatal) withdrawal symptoms. Tell your doctor immediately if you notice any signs with your newborn baby. Sobbing, slow/small breathing, irritability, shaking, nausea, diarrhea, poor or difficult food.
If using the aqueous form of this medication, use a measuring device to carefully measure the dose. Do not use a household spoon. Because then you will not get the correct dosage.
Dosage is based on your health status and response to healing. In children, the dose is also based on body weight. Do not increase your dose. Do not take the medication frequently. For example, if it is directed at you, take the medication the right way.
Ovarian medications work better when used at the first symptoms of pain. If you wait until the pain gets worse, the medication may not activate.
If you have persistent pain (through cancer, for example), your doctor may trust you to use on long-term opioid medications. In this case, this medication can only be used if needed for unexpected (breakthrough) pain. Other anesthetics (ibuprofen, naproxen, etc.) can still be prescribed. Ask your doctor or pharmacist about the non-problematic use of this medication in combination with other medications.
Stopping this medication abruptly can cause withdrawal, especially if you have been using it for a long time or at high doses. To prevent withdrawal, your doctor can slowly decrease the dosage. Tell your doctor or pharmacist right away if you get signs of withdrawal, such as agitation, mental/mood changes (including agitation, sleep disturbances, thoughts of suicide), vision loss, nausea, nausea, diarrhea, sweating, muscle pain, or sudden behavioral changes.
If this medication has been used for an extended period of time, it may not work. If this medication does not work completely, consult your doctor.
Although it can help almost all people, this drug can sometimes cause dependence. This risk may be higher if there is impairment in the use of the resource (e.g., excessive use or drug/alcohol addiction). Take this medication literally as prescribed to reduce the risk of addiction. Contact your physician or pharmacist for more information.
Tell your doctor if your pain does not get better or worse.
Side Effects
See also the Warnings section.
Nausea, nausea, blockage, lightheadedness, dizziness, or drowsiness may be preventable. Some of these side effects may diminish after you have been using this drug for some time. If one of these effects persists or worsens, tell your doctor or pharmacist immediately.
To prevent constipation, you should use fiber, drink plenty of water, and exercise. You may need to take a laxative. Ask your pharmacist which type of laxative is right for you.
To reduce the risk of head dizziness or lightheadedness, stand up slowly from a sitting or lying position.
Remember that this medication is prescribed because your doctor has ruled that the benefit outweighs the risk of side effects. Almost everyone using this medication has no serious side effects.
Tell your doctor immediately if you have any serious side effects such as breathing during sleep (sleep apnea), mental/mood forming (e.g., agitation, confusion, hallucinations), abdominal pain/abdominal pain, stomach pain, or urinary tract problems that prevent you from functioning. appropriately (e.g., loss of appetite, unusual fatigue, weight loss).
If you have persistent pain (through cancer, for example), your doctor may trust you to use on long-term opioid medications. In this case, this medication can only be used if needed for unexpected (breakthrough) pain. Other anesthetics (ibuprofen, naproxen, etc.) can still be prescribed. Ask your doctor or pharmacist about the non-problematic use of this medication in combination with other medications.
Very serious allergic reactions to this product are rare. If you notice signs of a severe allergic reaction, such as skin rash, itching / swelling (especially of the face / tongue / throat), strong dizziness, hateful breathing, etc., immediately seek medical assistance notwithstanding.
This is not an absolute list of possible adverse reactions. If you notice any other effects not mentioned above, contact your physician or pharmacist.
In the U.S., call your doctor for medical advice regarding side effects. 1-800-FDA-1088 or you can report side effects to the FDA at www. FDA.Gov/Medwatch.
For medical advice regarding side effects, call your Canadian physician at 1-866-234-2345 to report side effects to Health Canada.
Precautionary Measures
See also the warnings in the section
Tell your doctor or pharmacist before taking this medication if you are allergic to this medication or other opioids (such as benzidrocodone, hydromorphone, morphine, codeine); or if you have other allergies. This product contains inactive ingredients that may cause allergic reactions or other problems. Consult your pharmacist for further information.
Inform your own physician or pharmacist about this medication, especially about your own medical conditions: brain damage (head trauma, tumors, epileptic seizures, etc.), breathing difficulties (asthma, sleep apnea, symptoms obstructive lung disease, etc.), kidney disease), kidney disease), kidney disease) liver disease, psychiatric/mood disorders (e.g., loss, depression, suicidal thoughts), personal or domestic history of psychoactive drug use (e.g., excessive use of or dependence on drugs/alcohol), stomach/intestinal problems (e.g., blockages… (e.g., constipation, diarrhea due to infection, paralyzed ileum), urinary problems (e.g., due to an enlarged prostate gland), gallbladder problems, pancreatic (pancreatitis) problems.
This product may cause dizziness and drowsiness. Alcohol or marijuana (cannabis) can make you even more dizzy or sleepy. Do not drive, use a car, or do anything that requires caution unless it can be done safely. Be careful with alcoholic beverages. Consult your physician if you intend to use marijuana (cannabis).
Liquid products are more likely to contain sugar and alcohol. If you have diabetes, alcoholism, liver disease, or another condition that requires limiting/avoiding these drugs on the menu, a conversation is recommended. Ask your doctor or pharmacist about the non-trivial use of this product.
Precautionary Measures
If you have persistent pain (through cancer, for example), your doctor may trust you to use on long-term opioid medications. In this case, this medication can only be used if needed for unexpected (breakthrough) pain. Other anesthetics (ibuprofen, naproxen, etc.) can still be prescribed. Ask your doctor or pharmacist about the non-problematic use of this medication in combination with other medications.
Elderly persons may be sensitive to the side effects of this product, especially mal laziness, dizziness, drowsiness, and slow/small breathing.
During pregnancy, this drink may be used only as needed. It may be harmful to the fetus. Talk to your doctor about the risks and effects.
This medication turns into breast milk and may have unwanted effects on a nursing baby. Tell your doctor immediately if your baby is unusually sleepy, has difficulty eating, or experiences breathing problems. Consult your physician before breastfeeding.
Interacting.
See also the warnings in the section
Interactions between drugs can alter the effects of a drug or increase the risk of serious side effects. This document does not include all possible interactions between medications. Keep a list of all products you use (including prescription drugs or including prescription drugs and herbal products) and share it with your physician or pharmacist. Do not start, stop, or change the dosage of each medication without your physician’s permission.
Some products that can interact with this product are some anesthetics (mixed opioid agonists/antagonists such as butorphanol, nalbuphine, pentazocine) and samidorphan naltrexone).
Risk of serious side effects (e.g., slow breathing, drowsiness/ dizziness) may increase when taking medications with other products that may cause drowsiness or breathing problems. If you use other products, such as other opioid pain or cough medicines (e.g., codeine, oxycodone), alcohol, marijuana (cannabis), sleep or anxiety (e.g., alprazolam, lorazepam, zolpidem), muscle breakdown or pharmacist. cyclobenzaprine) or antihistamines (such as cetirizine or diphenhydramine).
Check the labels on all medications (e.g., allergy and cough medicines). Ask your pharmacist about the safe use of these products.
Other medications may affect the removal of hydrocodone/acetaminophen from your body. (carbamazepine, phenytoin), among others.
If you have persistent pain (through cancer, for example), your doctor may trust you to use on long-term opioid medications. In this case, this medication can only be used if needed for unexpected (breakthrough) pain. Other anesthetics (ibuprofen, naproxen, etc.) can still be prescribed. Ask your doctor or pharmacist about the non-problematic use of this medication in combination with other medications.
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