You may also need to take a laxative. Ask your pharmacist which type of laxative is right for you. To reduce the risk of dizziness and lightheadedness, get up slowly when rising from a sitting or lying position. Remember that this medication has been prescribed because your doctor has judged that the benefit to you is greater than the risk of side effects. Many people using this medication do not have serious side effects.
A very serious allergic reaction to this drug is rare. However, get medical help right away if you notice any symptoms of a serious allergic reaction, including:. This is not a complete list of possible side effects. If you notice other effects not listed above, contact your doctor or pharmacist.
Call your doctor for medical advice about side effects. In Canada - Call your doctor for medical advice about side effects. You may report side effects to Health Canada at Before taking this medication, tell your doctor or pharmacist if you are allergic to hydrocodone; or to homatropine; or to other opioid medications such as codeine, hydromorphone ; or if you have any other allergies.
This product may contain inactive ingredients, which can cause allergic reactions or other problems. Talk to your pharmacist for more details. Before using this medication, tell your doctor or pharmacist your medical history, especially of:. This drug may make you dizzy or drowsy or blur your vision. Alcohol or marijuana cannabis can make you more dizzy or drowsy. Do not drive, use machinery, or do anything that needs alertness or clear vision until you can do it safely.
Avoid alcoholic beverages. Talk to your doctor if you are using marijuana cannabis. Before having surgery, tell your doctor or dentist about all the products you use including prescription drugs, nonprescription drugs, and herbal products. During pregnancy, this product is not recommended. It may harm an unborn baby. Talk to your doctor about the risks and benefits of this medication. See also Warning section.
This product passes into breast milk and may have undesirable effects on a nursing infant such as unusual sleepiness, difficulty feeding, trouble breathing, or unusual limpness.
Breast-feeding while using this product is not recommended. Consult your doctor before breast-feeding. Drug interactions may change how your medications work or increase your risk for serious side effects. This document does not contain all possible drug interactions. Do not start, stop, or change the dosage of any medicines without your doctor's approval.
Tell your doctor or pharmacist if you are taking other products such as other opioid pain or cough relievers such as codeine, hydromorphone , alcohol, marijuana cannabis , drugs for sleep or anxiety such as alprazolam, lorazepam, zolpidem , muscle relaxants such as carisoprodol, cyclobenzaprine , or antihistamines such as cetirizine, diphenhydramine.
Check the labels on all your medicines such as allergy or cough-and-cold products because they may contain ingredients that cause drowsiness. Ask your pharmacist about using those products safely. Examples include azole antifungals such as ketoconazole , macrolide antibiotics such as erythromycin , mifepristone, HIV medications such as ritonavir , rifamycins such as rifabutin, rifampin , certain drugs used to treat seizures such as carbamazepine, phenytoin , among others.
Make sure laboratory personnel and all your doctors know you use this drug. If someone has overdosed and has serious symptoms such as passing out or trouble breathing, call Otherwise, call a poison control center right away.
US residents can call their local poison control center at Canada residents can call a provincial poison control center. This medication has been prescribed for your current condition only. Do not use it later for another condition unless told to do so by your doctor.
A different medication may be necessary in those cases. This medicine will add to the effects of alcohol and other CNS depressants medicines that can make you drowsy or less alert. Some examples of CNS depressants are antihistamines or medicine for allergies or colds, sedatives, tranquilizers, or sleeping medicine, other prescription pain medicine or narcotics, medicine for seizures or barbiturates, muscle relaxants, or anesthetics, including some dental anesthetics.
Check with your doctor before taking any of these medicines while you are using this medicine. If you think you or someone else may have taken an overdose of this medicine, get emergency help at once. Symptoms of an overdose include: extreme dizziness or weakness, trouble breathing, slow heartbeat or breathing, seizures, and cold, clammy skin. In case of an overdose, call your doctor right away. This medicine may be habit-forming.
If you feel that the medicine is not working as well, do not use more than your prescribed dose. Call your doctor for instructions. This medicine may make you dizzy or drowsy. Do not drive or do anything else that could be dangerous until you know how this medicine affects you.
Using narcotics for a long time can cause severe constipation. To prevent this, your doctor may direct you to take laxatives, drink a lot of fluids, or increase the amount of fiber in your diet. Be sure to follow the directions carefully, because continuing constipation can lead to more serious problems.
Dizziness, lightheadedness, or fainting may occur when you get up suddenly from a lying or sitting position. Getting up slowly may help lessen this problem. Also, lying down for a while may relieve the dizziness or lightheadedness. Using this medicine while you are pregnant may cause serious unwanted effects, including neonatal opioid withdrawal syndrome in your newborn baby. Tell your doctor right away if you think you are pregnant or if you plan to become pregnant while using this medicine.
This medicine may cause adrenal insufficiency. Check with your doctor right away if you have darkening of the skin, diarrhea, dizziness, fainting, loss of appetite, mental depression, nausea, skin rash, unusual tiredness or weakness, or vomiting. If you are especially sensitive to the effects of this medicine, do not suddenly stop using it without first checking with your doctor.
Your doctor may want you to gradually reduce the amount you are using before stopping it completely. This may help reduce the possibility of withdrawal symptoms, such as abdominal or stomach cramps, anxiety, fever, nausea, runny nose, sweating, tremors, or trouble sleeping. Using too much of this medicine may cause infertility unable to have children. Talk with your doctor before using this medicine if you plan to have children.
Make sure any doctor or dentist who treats you knows that you are using this medicine. This medicine may affect the results of certain medical tests. Do not take other medicines unless they have been discussed with your doctor.
This includes prescription or nonprescription over-the-counter [OTC] medicines and herbal or vitamin supplements. Along with its needed effects, a medicine may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention. Some side effects may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine.
Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects. Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them:. Tell your healthcare provider right away if you are pregnant or think you may be pregnant. Ask your healthcare provider if you have any questions about this information.
Before you take Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution, tell your healthcare provider about all of your medical conditions, including if you:. Tell your healthcare provider about all the medicines you take , including prescription and over-the-counter medicines, vitamins, and herbal supplements. Taking Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution with certain other medicines can cause side effects or affect how well Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution or the other medicines work.
Do not start or stop taking other medicines without talking to your healthcare provider. Ask your healthcare provider if you are not sure if you take one of these medicines. Call your doctor for medical advice about side effects. Remove unused Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution from the container and mix it with an undesirable, non-toxic substance such as cat litter or used coffee grounds to make it less appealing to children and pets.
Place the mixture in a container such as a sealed plastic bag and throw it away in the household trash. You can also follow your state or local guidelines on how to safely throw away Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution. General information about the safe and effective use of Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution. Medicines are sometimes prescribed for purposes other than those listed in a Medication Guide.
Do not use Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution for a condition for which it was not prescribed. Do not give Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution to other people, even if they have the same symptoms that you have. It may harm them.
You can ask your pharmacist or healthcare provider for information about Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution that is written for health professionals.
Active ingredients: hydrocodone bitartrate and homatropine methylbromide. This Medication Guide has been approved by the U. Food and Drug Administration. DailyMed will deliver notification of updates and additions to Drug Label information currently shown on this site through its RSS feed.
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Approval: Hydrocodone bitartrate and homatropine methylbromide oral solution exposes users to risks of addiction, abuse, and misuse, which can lead to overdose and death. Monitor closely, especially upon initiation or when used in patients at higher risk.
Avoid the use of hydrocodone bitartrate and homatropine methylbromide oral solution in patients taking CYP3A4 inhibitors or inducers. Avoid the use of hydrocodone bitartrate and homatropine methylbromide oral solution in patients taking benzodiazepines, other CNS depressants, or alcohol. Prolonged use of hydrocodone bitartrate and homatropine methylbromide oral solution during pregnancy can result in neonatal opioid withdrawal syndrome, which may be life- threatening if not recognized and treated.
If hydrocodone bitartrate and homatropine methylbromide oral solution is used for a prolonged period in a pregnant woman, advise the patient of the risk of neonatal opioid withdrawal syndrome and ensure that appropriate treatment will be available.
May increase intracranial pressure and obscure the clinical course of head injuries. Avoid use in patients with circulatory shock. Discontinue if serotonin syndrome is suspected. Monitor for reduced effect. May cause fetal harm. Life-Threatening Respiratory Depression Serious, life-threatening, or fatal respiratory depression may occur with use of hydrocodone bitartrate and homatropine methylbromide oral solution.
Accidental Ingestion Accidental ingestion of even one dose of hydrocodone bitartrate and homatropine methylbromide oral solution, especially by children, can result in a fatal overdose of hydrocodone [see Warnings and Precautions 5. Risk of Medication Errors Ensure accuracy when prescribing, dispensing, and administering hydrocodone bitartrate and homatropine methylbromide oral solution.
Cytochrome P 3A4 Interaction The concomitant use of hydrocodone bitartrate and homatropine methylbromide oral solution with all cytochrome P 3A4 inhibitors may result in an increase in hydrocodone plasma concentrations, which could increase or prolong adverse drug effects and may cause potentially fatal respiratory depression. Risks from Concomitant Use with Benzodiazepines or Other CNS Depressants Concomitant use of opioids with benzodiazepines or other central nervous system CNS depressants, including alcohol, may result in profound sedation, respiratory depression, coma, and death.
Interaction with Alcohol Instruct patients not to consume alcoholic beverages or use prescription or non-prescription products that contain alcohol while taking hydrocodone bitartrate and homatropine methylbromide oral solution. Neonatal Opioid Withdrawal Syndrome Hydrocodone bitartrate and homatropine methylbromide oral solution is not recommended for use in pregnant women [see Use in Specific Populations 8.
Hydrocodone bitartrate and homatropine methylbromide oral solution is contraindicated for: All children younger than 6 years of age [see Warnings and Precautions 5. Acute or severe bronchial asthma in an unmonitored setting or in the absence of resuscitative equipment [see Warnings and Precautions 5.
Known or suspected gastrointestinal obstruction, including paralytic ileus [see Warnings and Precautions 5. Hypersensitivity to hydrocodone, homatropine, or any of the inactive ingredients in hydrocodone bitartrate and homatropine methylbromide oral solution [see Adverse Reactions 6 ].
Asthma and Other Pulmonary Disease The use of hydrocodone bitartrate and homatropine methylbromide oral solution in patients with acute or severe bronchial asthma in an unmonitored setting or in the absence of resuscitative equipment is contraindicated [ s ee Contraindications 4 ]. The following serious adverse reactions are described, or described in greater detail, in other sections: Addiction, abuse, and misuse [see Warnings and Precautions 5. Other reactions include: Anaphylaxis : Anaphylaxis has been reported with hydrocodone, one of the ingredients in hydrocodone bitartrate and homatropine methylbromide oral solution.
Dermatologic : Flushing, hyperhidrosis, pruritus, rash. Musculoskeletal : Arthralgia, backache, muscle spasm. Ophthalmic : Miosis constricted pupils , visual disturbances. Reproductive : Hypogonadism, infertility. Other : Drug abuse, drug dependence, opioid withdrawal syndrome. Based on the animal data, advise pregnant women of the potential risk to a fetus.
Labor or Delivery Opioids cross the placenta and may produce respiratory depression and psycho-physiologic effects in neonates. Data Human Data Hydrocodone A limited number of pregnancies have been reported in published observational studies and postmarketing reports describing hydrocodone use during pregnancy.
Animal Data Reproductive toxicity studies have not been conducted with hydrocodone bitartrate and homatropine methylbromide; however, studies are available with individual active ingredients or related active ingredients.
H omatropine Animal studies with homatropine are not available. Hydrocodone Hydrocodone is present in breast milk. Homatropine No information is available on the levels of homatropine in breast milk or on milk production. Clinical Considerations Infants exposed to hydrocodone bitartrate and homatropine methylbromide through breast milk should be monitored for excess sedation and respiratory depression.
Risks Specific to Abuse of Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution Hydrocodone bitartrate and homatropine methylbromide oral solution is for oral use only. Treatment of Overdose Treatment of overdosage is driven by the overall clinical presentation, and consists of discontinuation of hydrocodone bitartrate and homatropine methylbromide oral solution together with institution of appropriate therapy.
Hemodialysis is not routinely used to enhance the elimination of hydrocodone from the body. Homatropine Homatropine is an anticholinergic that inhibits activity of the muscarinic acetylcholine receptor with less potency than atropine.
Effects on the Gastrointestinal Tract and Other Smooth Muscle Hydrocodone causes a reduction in motility associated with an increase in smooth muscle tone in the antrum of the stomach and duodenum. Effects on the Cardiovascular System Hydrocodone produces peripheral vasodilation which may result in orthostatic hypotension or syncope.
Effects on the Immune System Opioids have been shown to have a variety of effects on components of the immune system in in vitro and animal models.
Concentration—Adverse Reaction Relationships There is a relationship between increasing hydrocodone plasma concentration and increasing frequency of dose-related opioid adverse reactions such as nausea, vomiting, CNS effects, and respiratory depression. Homatropine Homatropine methylbromide has several mild but undesirable clinical properties resulting from its antisecretory effects.
Distribution Although the extent of protein binding of hydrocodone in human plasma has not been definitively determined, structural similarities to related opioid analgesics suggest that hydrocodone is not extensively protein bound. Excretion Hydrocodone and its metabolites are eliminated primarily in the kidneys.
Hydrocodone Carcinogenicity studies were conducted with codeine, an opiate related to hydrocodone. Mutagenicity studies with hydrocodone have not been conducted. Fertility studies with hydrocodone have not been conducted. Homatropine Carcinogenicity, mutagenicity, and fertility studies with homatropine have not been conducted. Dispense in a tight, light-resistant container as defined in the USP. Oral prescription where permitted by State Law.
Addiction, Abuse, and Misuse Inform patients that the use of hydrocodone bitartrate and homatropine methylbromide oral solution, even when taken as recommended, can result in addiction, abuse, and misuse, which can lead to overdose and death [see Warnings and Precautions 5. Important Dosing and Administration Instructions Instruct patients how to measure and take the correct dose of hydrocodone bitartrate and homatropine methylbromide oral solution.
Life-Threatening Respiratory Depression Inform patients of the risk of life-threatening respiratory depression, including information that the risk is greatest when starting hydrocodone bitartrate and homatropine methylbromide oral solution and that it can occur even at recommended dosages [see Warnings and Precautions 5. Accidental Ingestion Inform patients that accidental ingestion, especially by children, may result in respiratory depression or death [see Warnings and Precautions 5.
Activities Requiring Mental Alertness Advise patients to avoid engaging in hazardous tasks that require mental alertness and motor coordination such as operating machinery or driving a motor vehicle as hydrocodone bitartrate and homatropine methylbromide oral solution may produce marked drowsiness [see Warnings and Precautions 5.
Interactions with Benzodiazepines and Other Central Nervous System Depressants, Including Alcohol Inform patients and caregivers that potentially fatal additive effects may occur if hydrocodone bitartrate and homatropine methylbromide oral solution is used with benzodiazepines or other CNS depressants, including alcohol.
Constipation Advise patients of the potential for severe constipation [see Warnings and Precautions 5. Anaphylaxis Inform patients that anaphylaxis has been reported with ingredients contained in hydrocodone bitartrate and homatropine methylbromide oral solution. MAOI Interaction Inform patients not to take hydrocodone bitartrate and homatropine methylbromide oral solution while using or within 14 days of stopping any drugs that inhibit monoamine oxidase.
Hypotension Inform patients that hydrocodone bitartrate and homatropine methylbromide oral solution may cause orthostatic hypotension and syncope.
Pregnancy Advise patients that use of hydrocodone bitartrate and homatropine methylbromide oral solution is not recommended during pregnancy [see Use in Specific Populations 8.
Neonatal Opioid Withdrawal Syndrome Inform female patients of reproductive potential that use of hydrocodone bitartrate and homatropine methylbromide oral solution during pregnancy can result in neonatal opioid withdrawal syndrome, which may be life-threatening if not recognized and treated [see Warnings and Precautions 5.
Embryo-Fetal Toxicity Inform female patients of reproductive potential that hydrocodone bitartrate and homatropine methylbromide oral solution can cause fetal harm and to inform their healthcare provider of a known or suspected pregnancy [see Use in Specific Populations 8.
Lactation Advise women that breastfeeding is not recommended during treatment with hydrocodone bitartrate and homatropine methylbromide oral solution [see Use in Specific Populations 8. Infertility Inform patients that chronic use of opioids, such as hydrocodone, a component of hydrocodone bitartrate and homatropine methylbromide oral solution, may cause reduced fertility. Adrenal Insufficiency Inform patients that hydrocodone bitartrate and homatropine methylbromide oral solution could cause adrenal insufficiency, a potentially life-threatening condition.
Serotonin Syndrome Inform patients that hydrocodone bitartrate and homatropine methylbromide oral solution could cause a rare but potentially life-threatening condition resulting from concomitant administration of serotonergic drugs. Disposal of Unused Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution Advise patients to properly dispose of unused hydrocodone bitartrate and homatropine methylbromide oral solution.
Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution can cause serious side effects, including: Addiction, abuse and misuse. Taking Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution or other medicines that contain an opioid can cause addiction, abuse and misuse, which can lead to overdose and death.
This can happen even if you take Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution exactly as prescribed by your healthcare provider.
Your risk of addiction, abuse, and misuse is increased if you or a family member has a history of drug or alcohol abuse or addiction, or mental health problems. Life-threatening breathing problems respiratory depression. Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution can cause breathing problems respiratory depression that can happen at any time during treatment and can lead to death.
Your risk of breathing problems is greatest when you first start taking Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution, are taking other medicines that can cause breathing problems, have certain lung problems, are elderly, or have certain other health problems.
Children are at higher risk for respiratory depression. Breathing problems can happen even if you take Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution exactly as prescribed by your healthcare provider. Call your healthcare provider or get emergency medical help right away if anyone taking Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution has any of the symptoms below: increased sleepiness shallow breathing confusion limpness difficulty breathing Keep Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution in a safe place away from children.
Overdose and death due to medicine dosing errors. Overdose and death can happen if you measure the wrong dose of Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution. Always use an accurate milliliter mL measuring device to measure the correct amount of Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution. Do not use a household teaspoon to measure your medicine.
You may accidentally take too much. You can ask your pharmacist for the measuring device you should use and how to measure the correct dose. Breathing problems respiratory depression that can lead to death and opioid withdrawal can happen if you start taking or stop taking other medicines while taking Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution, including: certain antibiotics certain medicines to treat a fungal infection certain medicines to treat Human Immunodeficiency Virus HIV -1 infection, Acquired Immune Deficiency Syndrome AIDS , or Hepatitis C rifampin carbamazepine phenytoin Tell your healthcare provider if you take any of these medicines.
Severe drowsiness, breathing problems respiratory depression , coma, and death can happen in people who take Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution with benzodiazepines or other central nervous system depressants, including alcohol. Do not take benzodiazepines or any medicine that can cause drowsiness or sleepiness during treatment with Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution.
Do not drink alcohol or take prescription or over-the-counter medicines that contain alcohol during treatment with Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution.
Hydrocodone Bitartrate and Homatropine Methylbromide is a prescription medicine used in adults to treat a cough. Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution contain hydrocodone, an opioid narcotic cough suppressant. Hydrocodone Bitartrate and Homatropine Methylbromide is a federal controlled substance C - II because it contains hydrocodone that can be abused or lead to dependence.
Selling or giving away Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution may harm others, and is against the law. Tell your healthcare provider if you have ever abused or been dependent on alcohol, prescription medicines or street drugs.
See the end of this Medication Guide for a complete list of ingredients. Before you take Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution, tell your healthcare provider about all of your medical conditions, including if you: have a drug addiction have bile duct or pancreas problems have lung or breathing problems have glaucoma increased pressure in eyes have a fever and are coughing up mucus have prostate problems have had a recent head injury have problems with your urinary tract or difficulty urinating have had a brain tumor or other brain problems have kidney or liver problems have or have had seizures have adrenal gland problems have pain in your stomach-area abdomen have low blood pressure have constipation or other bowel problems plan to have surgery are pregnant or plan to become pregnant.
Hydrocodone passes into your breast milk and can cause serious side effects in your baby including increased sleepiness, breathing problems respiratory depression , and death. You and your healthcare provider should decide if you will take Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution or breastfeed. You should not do both. Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution may affect the ability to have a child in females and males fertility problems.
It is not known if these fertility problems will be reversible, even after you stop taking Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution. Talk to your healthcare provider if this is a concern for you. Especially tell your healthcare provider if you: take pain medicines such as opioids narcotics. Do not change your dose without talking to your healthcare provider.
If you do not have one, ask your pharmacist to give you a measuring device to help you measure the correct amount of Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution. You may accidently take too much. Do not overfill the measuring device. If you take too much Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution, call your healthcare provider or go to the nearest hospital emergency room right away.
Tell your healthcare provider if your cough does not get better within 5 days of treatment with Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution. Avoid driving a car or operating machinery during treatment with Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution.
Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution can cause you to be drowsy, slow your thinking and motor skills, and affect your vision. Drinking alcohol can increase your chances of having serious side effects. Use of Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution while breastfeeding can cause severe breathing problems respiratory depression in your breastfed infant that could be life-threatening.
Avoid the use of Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution if you have a head injury or have been told that you have changes in the tissue of your brain brain lesions or increased pressure in your head. Increased risk of seizures in people with seizure disorders. If you have a seizure disorder, Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution may increase how often you have a seizure.
Low blood pressure. A sudden drop in blood pressure can happen in some people during treatment with Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution and this may cause you to feel dizzy, faint, lightheaded, or weak, especially when you stand up orthostatic hypotension.
Your risk of having this problem may be increased if you take Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution with certain other medicines that lower blood pressure. If you have any of these symptoms while taking Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution, sit or lie down. Do not change your body position too fast. Get up slowly from sitting or lying down. Adrenal gland problems. Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution can cause serious and life-threatening adrenal gland problems.
Your healthcare provider may do blood tests to check for adrenal gland problems. Call your healthcare provider right away if you have any of these symptoms: nausea weakness vomiting dizziness not wanting to eat anorexia low blood pressure fatigue The most common side effects of Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution include: sleepiness dizziness confusion headache coordination problems dry mouth decrease in mental and physical performance nausea vomiting lack of energy lightheadedness constipation These are not all the possible side effects of Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution.
Store Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution in a tightly closed container, in a dry, cool place away from heat or direct sunlight. Keep Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution and all medicines out of the reach of children. One Pint mL. Version Files Oct 23, 24 current download Mar 20, 23 download Dec 13, 22 download Jan 17, 20 download Dec 6, 16 download Oct 3, 7 download Nov 27, 3 download Sep 19, 2 download Dec 23, 1 download.
NDC 1 Product Information. Inactive Ingredients.
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