DOXILAMINE AUROVITAS 25 mg FILM-COATED TABLETS

2. What you need to know before taking Doxilamine Aurovitas

Do not take Doxilamine Aurovitas

• If you are allergic to doxilamine or any of the other components of this medicine (listed in section 6).
• If you are allergic to other antihistamines (anti-allergics).
• If you are pregnant or breastfeeding.

Warnings and Precautions

Consult your doctor or pharmacist before starting to take Doxilamine Aurovitas.

You should consult a doctor before taking this medicine if you have:

• Liver and kidney function disorders.
• Epilepsy.
• QT interval prolongation (a heart problem).
• Low potassium levels in the blood or other electrolyte disturbances.
• Heart disease and high blood pressure.
• Asthma, chronic bronchitis (persistent inflammation of the bronchi), and pulmonary emphysema (a disease affecting the lungs, making breathing difficult).
• Glaucoma (increased eye pressure).
• Urinary retention.
• Prostatic hypertrophy (abnormal enlargement of the prostate).
• Peptic ulcer (erosion of the stomach or duodenal wall), pyloroduodenal obstruction (difficulty passing food from the stomach to the intestine), and obstruction of the bladder neck (urinary tract disease).

If you experience daytime drowsiness, it may be necessary to reduce the dose or take it earlier to ensure that at least 8 hours pass until waking time.

Alcohol consumption should be avoided during treatment.

If you are over 65 years old, you may be more susceptible to experiencing side effects.

Doxilamine Aurovitas may worsen dehydration symptoms and heat stroke due to decreased sweating.

Taking Doxilamine Aurovitas with Other Medicines

Inform your doctor or pharmacist if you are using, have recently used, or may need to use any other medicine.

Do not take Doxilamine Aurovitas with the following medicines, as their effects may be enhanced:

• Epinephrine (for low blood pressure).
• Medicines that act on the heart, such as those used to treat arrhythmias, some antibiotics, certain antimalarial drugs, certain antihistamines, certain lipid-lowering agents, or certain neuroleptics (medicines for treating mental disorders).
• Medicines that decrease the elimination of others, such as azole derivatives or macrolides, as they may increase the effect of Doxilamine Aurovitas.
• Certain diuretics (medicines that increase urine production).
• Central nervous system depressants (e.g., barbiturates, hypnotics, sedatives, anxiolytics, opioid analgesics, antipsychotics, or procarbazine).
• Antihypertensives (medicines for treating high blood pressure) with a central nervous system effect, such as guanabenz, clonidine, or alpha-methyldopa.
• Other anticholinergic drugs, such as medicines for treating depression or Parkinson's disease, monoamine oxidase inhibitors (medicines for depression), neuroleptics (medicines for treating mental disorders), atropine-like medicines for treating spasms, or disopyramide (for treating certain heart problems).
• If you are taking other medicines that can cause ear toxicity, such as carboplatin or cisplatin (cancer medicines), chloroquine (a medicine for treating or preventing malaria), and some antibiotics (medicines for treating infections) like erythromycin or injected aminoglycosides, among others; Doxilamine Aurovitas may mask the toxic effects of these medicines, so you should periodically review the condition of your ears.

Interference with Diagnostic Tests

Doxilamine may interfere with skin allergy tests using allergens. It is recommended to discontinue treatment with Doxilamine Aurovitas at least three days before starting such tests.

Taking Doxilamine Aurovitas with Food, Drinks, and Alcohol

Alcoholic beverages should not be consumed during treatment with Doxilamine Aurovitas. See section 3. How to take Doxilamine Aurovitas.

Pregnancy, Breastfeeding, and Fertility

Do not take Doxilamine Aurovitas if you are pregnant, plan to become pregnant, or are breastfeeding.

No data are available on the possible effects of Doxilamine Aurovitas on human fertility.

Driving and Using Machines

The influence of Doxilamine Aurovitas on the ability to drive and use machines is significant. Do not drive or use hazardous machinery while taking this medicine, at least during the first days of treatment, until you know how it affects you.

3. How to Take Doxilamine Aurovitas

Follow exactly the administration instructions of the medicine contained in this leaflet or as indicated by your doctor or pharmacist. In case of doubt, ask your doctor or pharmacist.

Adults (over 18 years)

The recommended dose is 1 tablet (25 mg) per day.

If daytime drowsiness occurs, it is recommended to reduce the dose to half a tablet (12.5 mg) per day or take it earlier to ensure that at least 8 hours pass until waking time.

Do not take more than 1 tablet (25 mg) per day.

Use in Adults over 65 Years

People over 65 years old are more prone to suffering from other conditions that may recommend a dose reduction. In case of unwanted side effects, it is recommended to reduce the dose to half a tablet (12.5 mg) per day.

Use in Patients with Liver or Kidney Disease

These patients should take a different dose, adjusted to the degree of their disease, which will be determined by the doctor.

Use in Children and Adolescents

Doxilamine Aurovitas is not recommended for use in children under 18 years old, so the medicine should not be used in this population.

Route and Method of Administration

Oral route.

The tablet can be divided into equal doses.

The tablets should be taken 30 minutes before bedtime with a sufficient amount of liquid (preferably water).

Duration of Treatment

The duration of treatment should be as short as possible. In general, the duration of treatment may range from a few days to a week.

It should not be administered for a period exceeding 7 days without consulting a doctor.

If You Take More Doxilamine Aurovitas Than You Should

The symptoms of an overdose are: drowsiness, depression or stimulation of the central nervous system, anticholinergic effects (dilated pupils, fever, dry mouth, decreased intestinal tone), flushing, increased or altered heart rate, increased blood pressure, nausea, vomiting, agitation, alteration of gait, dizziness, irritability, sedation, confusion, and hallucinations. Delirium, psychosis, decreased blood pressure, convulsions, decreased respiration, loss of consciousness, coma, and death may occur. A serious complication can be rhabdomyolysis (a muscle injury), followed by kidney failure.

There is no specific antidote for antihistamine overdose, so treatment is symptomatic and supportive. Your doctor will assess the need to induce vomiting, perform gastric lavage, or prescribe medicines to increase blood pressure if necessary.

In case of overdose or accidental ingestion, consult the Toxicological Information Service, phone: 91 562 04 20, indicating the medicine and the amount ingested.

If You Forget to Take Doxilamine Aurovitas

Do not take a double dose to make up for forgotten doses.

Take your dose at the usual time the next day.

If you have any other doubts about the use of this medicine, ask your doctor or pharmacist.

4. Possible Side Effects

Like all medicines, Doxilamine Aurovitas can cause side effects, although not everybody gets them.

The side effects of doxilamine are, in general, mild and transient, being more frequent in the first days of treatment.

Common side effects (may affect up to 1 in 10 people): drowsiness and effects such as dry mouth, constipation, blurred vision, urinary retention, increased bronchial secretion, vertigo, dizziness, headache, pain in the upper abdominal area, fatigue, insomnia, and nervousness.

Uncommon side effects (may affect up to 1 in 100 people): asthenia (fatigue), peripheral edema (inflammation of arms and legs), nausea, vomiting, diarrhea, skin rash, tinnitus (ringing in the ears), orthostatic hypotension (decrease in blood pressure due to postural changes), diplopia (double vision), dyspepsia (stomach disorders), feeling of relaxation, nightmares, and dyspnea (breathing difficulties).

Rare side effects (may affect up to 1 in 1,000 people): agitation (especially in children and the elderly), tremors, convulsions, or blood disorders such as hemolytic anemia, thrombocytopenia, leukopenia, or agranulocytosis (decrease in certain blood cells).

Side effects of unknown frequency (their frequency cannot be estimated from the available data): general malaise.

Other side effects that have occurred with the use of antihistamines in general, although not observed with doxilamine, are the following: arrhythmia (alteration of heart frequency), palpitations, duodenogastric reflux, abnormal liver function (cholestatic jaundice), prolonged QT interval on the electrocardiogram (a cardiac disorder), decreased appetite, increased appetite, myalgia (muscle pain), abnormal coordination, extrapyramidal disorder (movement disorders), paresthesia (abnormal sensations), impairment of psychomotor activities (senses-movement coordination), depression, decreased bronchial secretion, alopecia (hair loss), allergic dermatitis, hyperhidrosis (excessive sweating), photosensitivity reaction, or hypotension (low blood pressure).

The frequency and magnitude of side effects may be reduced by decreasing the daily dose.

People over 65 years old have a higher risk of experiencing adverse reactions, as they may have other diseases or may be taking other medicines simultaneously. These people also have a higher risk of falling.

Reporting of Side Effects

If you experience any side effects, consult your doctor or pharmacist, even if it is a possible side effect not listed in this leaflet. You can also report them directly through the Spanish Pharmacovigilance System for Human Use Medicines: www.notificaRAM.es. By reporting side effects, you can contribute to providing more information on the safety of this medicine.

5. Storage of Doxilamine Aurovitas

No special storage conditions are required.

Keep this medicine out of the sight and reach of children.

Do not use this medicine after the expiry date stated on the packaging after "EXP". The expiry date is the last day of the month indicated.

Medicines should not be disposed of via wastewater or household waste. Place the packaging and any unused medicines in the pharmacy's SIGRE collection point. If in doubt, ask your pharmacist how to dispose of the packaging and any unused medicines. This will help protect the environment.

6. Contents of the Pack and Further Information

Composition of Doxilamine Aurovitas

The active ingredient is doxilamine. Each tablet contains 25 mg of doxilamine hydrogensuccinate.

The other ingredients are:

Tablet core: microcrystalline cellulose, calcium hydrogen phosphate dihydrate, low-substituted hydroxypropylcellulose, colloidal silica, and magnesium stearate.

Tablet coating: hypromellose, titanium dioxide (E-171), macrogol 6000, talc, and indigo carmine lake (E-132).

Appearance of the Product and Contents of the Pack

Doxilamine Aurovitas 25 mg is presented in the form of film-coated tablets of blue color, oblong, and scored. Each pack contains 7 and 14 tablets.

Marketing Authorization Holder

Aurovitas Spain, S.A.U.

Avda. de Burgos, 16-D

28036 Madrid

Spain

Phone: 91 630 86 45

Fax: 91 630 26 64

Manufacturer

Laboratorios Normon, S.A.

Ronda de Valdecarrizo, 6 – 28760 Tres Cantos – Madrid (SPAIN)

Date of the Last Revision of this Leaflet: February 2015

Detailed and updated information on this medicine is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es/