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Oxazepam Teva

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Oxazepam Teva

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Medically reviewed

Marina Burgos

Last updated on 10/01/2026

This page provides general, reference-level information compiled from official medical sources. It is not a substitute for professional medical advice, diagnosis, or treatment. For decisions about your health, please consult a qualified healthcare professional.

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Overview of Oxazepam Teva

Quick Facts

Property Description
Active ingredient Oxazepam
Form Tablet or Capsule (Oral)
Pharmacological class Benzodiazepine (CNS Depressant)
General purpose Relief of anxiety and tension
Origin Synthetic compound

Oxazepam Teva is a medicine containing the active substance oxazepam, a synthetic compound that is classified as a benzodiazepine. The medication, manufactured by Teva, is typically supplied in solid dosage forms, such as a tablet or capsule, intended for oral intake. Belonging to the class of central nervous system (CNS) depressants, oxazepam’s primary effect is to modulate and reduce excessive nerve activity in the brain.

This benzodiazepine is used to address conditions involving high levels of mental and physical stress. For instance, oxazepam is clinically recognized for the short-term relief of the symptoms of anxiety disorders and is also indicated for managing acute symptoms related to alcohol withdrawal. This medication helps to calm the nervous system and relieve states of intense anxiety, often positioning it for adult patients experiencing significant stress or agitation.

Oxazepam is characterized as an intermediate-acting agent within its class, distinguishing its duration of effect from both shorter-acting and longer-acting analogues. Within regulatory frameworks, oxazepam is a Schedule IV controlled substance, which emphasizes its potent nature and the necessity of appropriate medical oversight. As a prescription-only medicine, the use of Oxazepam Teva requires strict supervision by a qualified healthcare professional.

Regulatory References

  1. Oxazepam - StatPearls - NCBI Bookshelf - NIH
  2. Label: OXAZEPAM capsule - DailyMed - NIH
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What side effects are possible with Oxazepam Teva?

Possible Side Effects and Safety Information

The safety profile of oxazepam is characterized by effects primarily related to its central nervous system (CNS) depressant activity, as documented in official regulatory labeling. These adverse reactions are classified by frequency and the body system affected.

Documented Adverse Reactions

The most common or expected adverse reactions officially listed in regulatory documents include drowsiness, dizziness, vertigo, headache, and hypotension (low blood pressure). These effects are especially noted at the initiation of treatment.

Adverse reactions are grouped by system-organ class, with effects predominantly occurring in the Nervous System Disorders (e.g., ataxia, decreased alertness) and Psychiatric Disorders (e.g., confusion, slurred speech, agitation).

Serious Safety Concerns

Official labeling emphasizes several serious safety concerns. The most critical is the risk of severe CNS depression, including respiratory depression, coma, and death, particularly when used with other CNS depressants. Furthermore, oxazepam exposes users to the risks of abuse, misuse, and addiction.

Physical and psychological dependence can develop, even when the medicine is used as prescribed. The risk of dependence increases with longer treatment duration, potentially leading to life-threatening acute withdrawal reactions upon rapid discontinuation.

Population-Specific Notes

Older adults (geriatric patients) are officially noted as being more sensitive to CNS effects like severe drowsiness, dizziness, and hypotension. Use during late pregnancy is associated with the risk of Neonatal Sedation and Withdrawal Syndrome in the newborn, according to regulatory documents.

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Overdose and Emergency Response

The official regulatory documents state that an overdose of Oxazepam is primarily characterized by Central Nervous System (CNS) depression. Documented manifestations in milder presentations include somnolence, confusion, slurred speech, and ataxia (impaired coordination).

In severe cases, the overdose may progress to more serious outcomes, including stupor, coma, profound respiratory depression (slowed or absent breathing), and hypotension (low blood pressure). Immediate medical attention must be sought for any suspected overdose, as the presence of any symptoms, particularly those involving consciousness or breathing, requires urgent evaluation.

The risk of severe outcomes, including death, is officially documented to be significantly increased when Oxazepam is ingested in combination with other CNS depressants, such as alcohol or opioids. Geriatric patients are noted to exhibit increased sensitivity to the sedative effects of an overdose.

Management in a healthcare setting is strictly symptomatic and supportive care. While flumazenil is a competitive receptor antagonist listed as an available antidote, its use is subject to regulatory constraints due to the documented risk of precipitating seizures, especially in patients with chronic use or mixed overdoses. Vigilant monitoring of vital signs is required.

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Therapeutic Uses of Oxazepam Teva

What Oxazepam Teva Treats: Main Uses and Benefits

The therapeutic utility of Oxazepam Teva is focused on providing support for conditions characterized by patient distress and heightened physiological activity. The medication is commonly applied in clinical settings that involve acute or unstable symptom patterns, where supportive symptom management is considered relevant.

Its core applications fall into certain specific domains: the management of symptoms associated with anxiety disorders and the treatment of acute alcohol withdrawal syndrome. It is commonly used to help with symptom clusters that interfere with daily comfort, such as excessive worry, uncontrollable restlessness, physical tension, and tremor.

Treatment Focus and Symptomatic Relief

The medication contributes to easing the overall symptom load for patients experiencing these manifestations. As a therapeutic benefit, it may help patients cope more steadily with symptom fluctuations during challenging symptomatic phases.

“The primary role of Oxazepam is to provide symptomatic support during periods of high physiological strain or acute emotional distress.”

  • Quick Fact: Supportive Role in Symptom Management Oxazepam is relevant for easing symptoms that interfere with daily comfort, including severe agitation, tension, and the physical signs of withdrawal.

This supportive therapy is applied when short-term symptomatic assistance is needed to address pronounced symptoms like irritability and acute tension in adults, including geriatric patients.

Regulatory References

  1. NIH DailyMed Official Label
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Eligibility and Restrictions for Use

The eligibility for using Oxazepam Teva is strictly defined by regulatory authorities and centers on age, underlying health conditions, and physiological status.

Populations for Whom Use is Contraindicated

Use is absolutely prohibited (contraindicated) for patients with a known hypersensitivity reaction to oxazepam or any other benzodiazepine compound. Furthermore, the medicine is not indicated for patients diagnosed with psychoses or acute pulmonary insufficiency.

Age- and Life-Stage Eligibility

The medicine is approved for use in adults and older adults. However, safety and effectiveness have not been established in pediatric patients under 6 years of age. Use in children between 6 and 12 years is restricted, as the absolute dosage is not established by U.S. labeling. Use is not recommended during pregnancy (especially the first and last trimesters) or while breastfeeding.

Conditions Requiring Restriction or Caution

Official labeling imposes restrictions for specific health profiles. Patients with a history of alcohol or drug abuse require careful surveillance due to the risk of dependence. The medicine must be administered with caution to depressed patients and to older adults or individuals where a sudden drop in blood pressure could lead to cardiac complications. The effectiveness of long-term use (beyond four months) has not been assessed by systematic clinical studies.

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What should I know about interactions with other medicines?

Interactions with other medicines and products

The official regulatory profile for Oxazepam is primarily defined by two interaction domains: additive pharmacodynamic (PD) effects and pharmacokinetic (PK) modifications of plasma exposure.

Pharmacodynamic Enhancement and Restrictions

Co-administration with other Central Nervous System (CNS) Depressants results in an enhancement of sedative effects. This includes medicines such as Opioids, antipsychotics, antidepressants, and sedative antihistamines. The co-use of Opioids and oxazepam is subject to a regulatory Boxed Warning due to the serious risk of profound sedation, respiratory depression, coma, and death. Concomitant intake of Alcohol is also not recommended due to the documented enhancement of sedative effects. Concurrent use with Antihypertensives may result in enhanced hypotensive effects.

Exposure Modification

Oxazepam plasma levels can be officially altered by other substances. Drugs that may cause oxazepam serum levels to fall include Rifampicin, Phenytoin, and Oestrogen-containing contraceptives. Conversely, the clearance of oxazepam may be reduced, potentially increasing its effects and the possibility of excessive sedation, when co-administered with a substance like Probenecid. An interaction is also documented with Levodopa, where concurrent use may decrease its therapeutic effects. Population-specific cautions exist for elderly patients, where co-administration with muscle relaxants may increase the risk of falling due to an accumulative muscle-relaxing effect.

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Mechanism of Action

How Oxazepam Teva Works

The mechanism of oxazepam is defined by its role as a Positive Allosteric Modulator (PAM), acting exclusively within the central nervous system (CNS) to enhance inhibitory signaling. The drug targets the Gamma-aminobutyric acid type A receptor ( GABA A receptor) complex, binding to a specific site distinct from the binding site of the natural GABA neurotransmitter.

This allosteric interaction increases the frequency of the GABA A receptor's chloride ion channel opening. The resulting influx of negatively charged chloride ions ( Cl^- influx) causes the postsynaptic neuronal membrane to become hyperpolarized.

This cellular consequence significantly reduces the excitability of the neuron, requiring a stronger signal to generate an electrical impulse. This generalized dampening of neuronal activity across central pathways, including the Limbic System and motor regions, initiates a systemic state of functional CNS depression. The physiological outcome is characterized by decreased central nervous system responsiveness and reduced muscle tension.

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Dosage and Administration Information

The medicine Oxazepam Teva is designed for oral administration, typically supplied as a tablet or a capsule in standard unit strengths of 10 mg, 15 mg, and 30 mg. Usage is strictly governed by prescribed schedules that require the total daily amount to be taken in divided doses, commonly administered three or four times per day. The medication may be taken with or without food.

The specific dosage is determined by the indication being addressed. For mild-to-moderate anxiety, the typical dose ranges from 10 mg to 15 mg per administration. For severe agitation, more pronounced anxiety syndromes, or in the context of acute alcohol withdrawal, the dose generally ranges from 15 mg to 30 mg per administration. The total daily dosage should generally not exceed 120 mg.

Administration is designated for short-term use only, and the effectiveness of treatment extending beyond four months has not been systematically established in clinical trials. Due to this short-term restriction, the process of discontinuing treatment is a procedural step that requires the dosage to be tapered gradually over a period of time, rather than stopped abruptly.

For specific patient populations, dosage modifications are a part of standardized use protocols. Older adults and debilitated patients are typically started on a lower regimen of 10 mg three times daily, with any subsequent increases being managed cautiously. The use of this medicine is not recommended for children under the age of six.

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Recent Clinical Evidence

Research evidence / Overview of studies for Oxazepam Teva

Evidence for Use in Anxiety Disorders and Tension

Research was studied for its use in conditions characterized by fluctuating or episodic manifestations of anxiety, tension, agitation, and irritability. The evidence base includes short-term, controlled studies, sometimes comparing oxazepam to a placebo or other active agents. These studies was evaluated in trials relevant in trials assessing short-term or episodic symptom patterns. Researchers monitored outcomes describing episodic or acute changes using standardized scales to track symptom intensity or variability.

Findings describe patterns observed in the studies related to outcomes capturing phases of heightened symptom activity. Studies report how symptoms evolved in the observed populations related to patient-reported outcomes describing perceived discomfort. Studies monitored short-term changes in these symptom patterns; findings describe group patterns, not personal outcomes.

Evidence for Use in Acute Alcohol Withdrawal Syndrome

Oxazepam was evaluated in research settings focused on the acute evaluation of symptoms associated with alcohol withdrawal, which is a condition associated with acute or disruptive episodes and temporary physiological imbalance. The studies primarily consisted of controlled comparative trials and systematic reviews, monitoring outcomes related to episodic or acute changes in symptom severity.

Studies monitored outcomes capturing phases of heightened symptom activity, using tools that measure symptom intensity or variability, such as the CIWA-Ar scale. Data show patterns related to how quickly and to what degree symptoms evolved in the observed populations. Studies monitored short-term changes in these symptom patterns, though evidence quality varies across studies.

Long-Term Studies and Follow-Up Data

Research was studied for its evidence structure related to short-term use. Follow-up durations were limited in the key studies because the medication was evaluated in trials assessing short-term or episodic symptom patterns. Long-term effects are not fully established. Clinical studies systematically assessing the use of this medication for periods longer than four months have not been performed. The available evidence is limited regarding the durability of any observed patterns or the outcomes related to extended use.

What Research Still Identifies as Uncertain

Research describes what is known—and what is still uncertain. In some of the older research, sample sizes were modest, and evidence quality varies across studies. This variability means that findings describe group patterns, not personal outcomes, and research does not determine whether an individual will respond similarly.

A major limitation is that long-term effects are not fully established, as the follow-up durations were limited in most relevant clinical trials. The results apply only to the populations studied and reflect the specific conditions under which they were conducted, meaning comparative evidence is lacking for certain head-to-head comparisons against newer or alternative treatments.

Key Studies & References

  1. Label: OXAZEPAM capsule, gelatin coated - DailyMed (Regulatory and Indication Status)
  2. Oxazepam - StatPearls (NIH) (Indications, Metabolism, and Use in Special Populations like the Elderly)
  3. Benzodiazepines in generalized anxiety disorder: heterogeneity of outcomes based on a systematic review and meta-analysis of clinical trials
  4. A 5-year follow-up study of users of benzodiazepine: starting with diazepam versus oxazepam (Long-term use patterns and dose escalation)
  5. Alcohol withdrawal syndrome in medical patients - Cleveland Clinic Journal of Medicine (CIWA-Ar scale and benzodiazepine options for AWS)
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Frequently Asked Questions (FAQ)

Common questions about Oxazepam Teva (FAQ)


Q: How quickly does Oxazepam Teva usually start to work?

Regulatory documents state that oxazepam is classified as having a relatively slow onset of action compared to some other medicines in its class. Peak levels of the medicine in the blood are generally reported to occur about three hours after taking an oral dose.


Q: How long does the effect of Oxazepam Teva typically last?

Oxazepam is classified as an intermediate-acting agent. The time it takes for the amount of oxazepam in the blood to be reduced by half (known as the mean elimination half-life) is approximately 8.2 hours.


Q: Can Oxazepam Teva cause dependence or addiction?

Yes, official regulatory labeling designates oxazepam as a Schedule IV controlled substance. This means the medicine carries a potential risk of abuse, misuse, and addiction. Physical and psychological dependence can develop even when the medicine is used exactly as prescribed.


Q: Is it common to feel very sleepy or drowsy on Oxazepam Teva?

Yes, drowsiness is one of the most frequent adverse reactions, especially at the start of treatment. Official information describes transient mild drowsiness as common in the first few days of therapy due to the medicine’s central nervous system depressant activity.


Q: What are the most common side effects of Oxazepam Teva?

According to official regulatory documents, the most common or expected adverse reactions include drowsiness, dizziness, vertigo, headache, and hypotension (low blood pressure).


Q: What substances should definitely be avoided when taking Oxazepam Teva?

Regulatory warnings specifically caution against the use of alcohol and opioids while taking oxazepam. Co-use with opioids is subject to a regulatory Boxed Warning due to the serious risk of severe sedation, respiratory depression, coma, and death. Alcohol intake is not recommended due to enhanced sedative effects.


Q: What is the risk of withdrawal symptoms from Oxazepam Teva?

The risk of physical dependence and subsequent withdrawal increases with longer treatment duration. Stopping the medicine abruptly can lead to acute withdrawal reactions, which can be life-threatening. Official protocols involve the dosage being tapered gradually over a period of time.


Q: Is Oxazepam Teva safe to use during pregnancy?

Official regulatory documents generally state that use during pregnancy is not recommended. Use during late pregnancy is associated with a specific risk of Neonatal Sedation and Withdrawal Syndrome in the newborn.


Q: Can a mother take Oxazepam Teva while breastfeeding?

Official product information states that oxazepam is found to be excreted into breast milk. Due to the potential for adverse effects in nursing infants (e.g., sedation), regulatory documents state a decision should be made whether to discontinue nursing or discontinue the drug.


Q: Is Oxazepam Teva the same as other 'pams' like lorazepam or diazepam?

Oxazepam belongs to the same class of medicines (benzodiazepines), but it is not identical to others like lorazepam or diazepam. Official sources classify oxazepam as an intermediate-acting agent distinguished by its slower onset of action and its primary metabolism route in the body.


Q: What's the difference between Oxazepam Teva and similar drugs mentioned online?

A key difference noted in regulatory data is that oxazepam uses a direct metabolic pathway called glucuronidation in the body. This specific characteristic may make it less likely to accumulate in individuals who have certain types of impaired liver function compared to other benzodiazepines.


Q: Why is Oxazepam Teva sometimes prescribed for alcohol withdrawal?

The medicine is officially indicated for the management of acute symptoms related to alcohol withdrawal. As a Central Nervous System (CNS) depressant, its effect helps to manage and reduce the over-excitation of the nervous system that is experienced during this acute withdrawal process.


Q: Are there any common over-the-counter medicines that interact with Oxazepam Teva?

While the focus is on prescription drugs, official interaction checkers note that oxazepam may affect the metabolism of certain over-the-counter pain relievers, such as acetaminophen. The co-use of oxazepam with opioid pain relievers carries a serious regulatory Boxed Warning.


Q: Does Oxazepam Teva affect birth control pills?

Regulatory documents indicate that oestrogen-containing oral contraceptives may influence how the body processes oxazepam. Specifically, they may cause oxazepam serum levels to fall, which could potentially reduce the medicine’s expected effects.


Q: Is Oxazepam Teva suitable for people with liver problems?

The medicine must be used with caution in patients with liver disease or impairment. However, because oxazepam is metabolized directly via glucuronidation, it is sometimes cited as having advantages over other benzodiazepines in individuals with certain impaired liver functions.


Q: What does the research say about Oxazepam Teva for generalized anxiety?

Official indications list the use of the medicine for the management of anxiety disorders and anxiety associated with tension, agitation, or irritability. The evidence base includes short-term, controlled studies relevant to managing these episodic manifestations of anxiety.


Q: Are there any studies on the long-term effects of Oxazepam Teva?

Official regulatory documents state that the effectiveness of treatment extending beyond four months has not been systematically established in clinical trials. Long-term effects are not fully established, and follow-up durations in key studies were limited.


Q: Why do some people say Oxazepam Teva is less potent than other benzodiazepines?

The perception of lower potency is likely based on official dose conversion resources. These resources often indicate that a higher milligram dose of oxazepam is required to achieve an equivalent therapeutic effect compared to an equal milligram dose of some other benzodiazepines.


Q: Is it normal to feel dizzy after taking Oxazepam Teva?

Yes, dizziness and vertigo are listed among the most common adverse reactions. Official documentation notes that these effects are especially noted at the initiation of treatment.


Q: Can you drive or operate machinery while taking Oxazepam Teva?

Due to the risk of drowsiness, dizziness, and decreased alertness, patients are generally warned against engaging in activities requiring complete mental alertness, such as operating machinery or driving a motor vehicle, due to the potential for impairment.


Q: What should be done if a dose of Oxazepam Teva is missed?

Official patient information often describes a general procedure: that a missed dose may be taken as soon as possible unless it is near the time for the next scheduled dose. Patients are generally cautioned not to take a double dose to make up for a missed one.


Q: Are there any known interactions with herbal supplements and Oxazepam Teva?

Some drug interaction databases note potential interactions with certain herbal products. For instance, supplements like St. John's Wort may reduce the medicine's effectiveness, while others like valerian root may increase its sedative effects.


Q: Does Oxazepam Teva affect blood pressure?

Yes, hypotension (low blood pressure) is listed as a common adverse reaction associated with the medicine. Official documentation states that the drug must be used with caution in individuals where a sudden drop in blood pressure could lead to cardiac complications.


Q: What is the primary way Oxazepam Teva leaves the body?

The medicine is primarily metabolized (broken down) in the liver via a process called glucuronidation. The resulting inactive components are then cleared from the body, mainly through excretion in the urine.


Q: Why are there different brands of oxazepam?

Oxazepam is the active generic ingredient in the medicine. The name 'Teva' is the name of the pharmaceutical company that manufactures and markets this specific product. It is common for the same generic medicine to be available under different brand names from various manufacturers.


Q: Does Oxazepam Teva make you feel 'high' or euphoric?

Official labeling notes the drug's potential for abuse and misuse. While not an expected therapeutic effect, the co-use with other Central Nervous System depressants, such as opioids, can enhance the effects, leading to an increased risk of psychological dependence.


Q: Is Oxazepam Teva used for sleep problems?

The official uses of oxazepam are for anxiety and alcohol withdrawal. However, because the medicine has sedative properties, some clinical contexts describe it as relevant for patients who experience difficulties with staying asleep.


Q: Can Oxazepam Teva cause changes in mood or personality?

Adverse reactions are officially listed under Psychiatric Disorders and include effects like confusion, slurred speech, and agitation. Additionally, mild paradoxical reactions (such as excitement or stimulation) have been reported in some patients.


Q: Can I take Oxazepam Teva if I have kidney issues?

Patients with kidney disease or impairment should use the medicine with caution. Monitoring is necessary, though because the medicine is primarily cleared from the body via the liver through glucuronidation, dose adjustments may not be as critical as with other medications.


Q: How does Oxazepam Teva affect memory?

The medicine's official safety profile lists effects on memory. Due to its Central Nervous System depressant activity, adverse effects such as memory impairment are associated with its use.


Q: Are there any special warnings for children or adolescents using Oxazepam Teva?

Safety and effectiveness have not been established in pediatric patients under 6 years of age. For children between 6 and 12 years, use is restricted as the absolute dosage is not established in regulatory documents.


Q: Does Oxazepam Teva have a risk of paradoxical reactions (opposite effect)?

Yes, official adverse reaction documentation reports that mild paradoxical reactions have been observed. These may include feelings of excitement or stimulation of affect, particularly in psychiatric patients, typically occurring early in therapy.


Q: What is meant by the half-life of Oxazepam Teva?

The term half-life is a scientific measure that describes the time it takes for the concentration of the medicine in the blood to decrease by half. Oxazepam has a mean elimination half-life of approximately 8.2 hours.


Q: Does Oxazepam Teva cause weight gain or loss?

Official drug labels do not commonly list weight change as a frequent or major adverse reaction. However, as with many psychiatric medications, some medical literature suggests that monitoring for potential weight changes may be a general consideration.


Q: Can people with breathing problems use Oxazepam Teva?

Official regulatory documents state that use is contraindicated (prohibited) for patients with acute pulmonary insufficiency. Due to its Central Nervous System depressant activity, the drug carries a risk of respiratory depression.


Q: What does official guidance say about using Oxazepam Teva before surgery?

Clinical guidelines generally describe the standard procedure: that patients may continue the medicine before surgery. The surgical team should be informed of the medication and dose so that anesthetic and analgesic doses can be considered for adjustment due to the potential for enhanced sedative effects.


Q: Is the risk of side effects higher at the beginning of treatment?

Yes, common adverse reactions such as drowsiness, dizziness, and headache are officially listed as being especially noted at the initiation of treatment.


Q: Does Oxazepam Teva interact with common pain relievers?

Official drug interaction databases note a potential interaction with acetaminophen. More critically, the co-use of oxazepam with opioid pain relievers carries a serious regulatory Boxed Warning for severe respiratory depression.


Q: Why is monitoring needed when taking Oxazepam Teva?

Monitoring is necessary due to the potential for adverse effects and signs of toxicity. It is also required due to the risk of drug abuse, misuse, and dependence. Patients using the drug with opioids require vigilant monitoring for respiratory compromise.


Q: Is Oxazepam Teva suitable for treating acute panic attacks?

Official indications list its use for anxiety disorders and anxiety with episodic manifestations. However, high-potency benzodiazepines are the only ones specifically approved by the U.S. FDA for the treatment of panic disorder.


Q: Are there any genetic factors that affect how Oxazepam Teva works?

While the medicine's primary metabolism route is less variable than other drugs, some medical literature suggests that genetic variability may play a part in certain idiosyncratic reactions to benzodiazepines, though this is not a universal finding.


Q: What happens if you suddenly stop taking Oxazepam Teva?

Stopping the medicine abruptly can lead to acute withdrawal reactions, which can be life-threatening. Official use protocols involve the dosage being tapered gradually over a period of time to reduce this risk.


Q: Is Oxazepam Teva used to relax muscles?

Yes, one of the physiological outcomes of the medicine's mechanism of action as a Central Nervous System (CNS) depressant is reduced muscle tension. Co-use with other muscle relaxants is cautioned due to a potential increase in the risk of falling.

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How should Oxazepam Teva be stored and disposed of?

How to Store and Dispose of Oxazepam Teva

Oxazepam must be stored under specific environmental conditions to maintain its quality and prevent misuse as a controlled substance.

Storage Requirements

Requirement Description
Temperature Store at controlled room temperature, typically 68 F to 77 F (20 C to 25 C).
Protection Keep away from excess heat and moisture and protect from light.
Container Keep in the original container and ensure it is tightly closed.
Security Store in a safe place and out of the reach of children.

Disposal Instructions

Unused or expired Oxazepam should not be kept. Patients are instructed to ask a healthcare professional or pharmacist for guidance on proper disposal. Due to its status as a controlled substance, authorized drug take-back programs are the recommended disposal method.

Attention! Always consult to a doctor or pharmacist before using pills or medicines.

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