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Almazine (Lorazepam)

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Almazine is a benzodiazepine medication. It is used to treat anxiety disorders, trouble sleeping, active seizures including status epilepticus, alcohol withdrawal. It is used to treat chemotherapy induced nausea and vomiting, as well as for surgery to interfere with memory formation and to sedate those who are being mechanically ventilated. While it can be used for severe agitation, midazolam is usually preferred. It is also used, along with other treatments, for acute coronary syndrome due to cocaine use. It can be given by mouth or as an injection into a muscle or vein. When given by injection onset of effects is between one and thirty minutes and effects last for up to a day.

Other names for this medication:
Almazine, Anxilor, Anxipose, Atipam, Biokalm, Biolar, Calmese, Dulozep, Larosh, Larpose, Lopam, Lopez, Lorakar, Loralite, Lorazam, Lorazepam, Lorazine, Loricon, Lorivan, Lorpam, Lorvin, Lotweet, Nexlor, Norpose, Olraz, Trapex, Urpam, Zepnap

Similar Products:
Omnicef, Thorazine, Rocaltrol, Pamelor, Plavix, Depakote, Prodine, Permisol, Priligy, Mebendex, Hynorm, Fluconal, Klosartan,

Also known as: Lorazepam


Almazine belongs to a class of medications called benzodiazepines. These medications work by boosting the activity of gamma-aminobutyric acid (GABA) within your body.

GABA is a neurotransmitter that transmits messages between cells in different parts of your body. Increasing GABA in the body results in a tranquilizing effect that reduces feelings of stress and anxiety.

How long does it take to work?

Benzodiazepines such as Almazine are categorized based on how fast they work. Almazine is classified as having a rapid to intermediate onset (start) of action. It begins to work right away after it’s taken, but its peak effect occurs within 1 to 1.5 hours.


When given intramuscularly, Almazine Injection, undiluted, should be injected deep in the muscle mass.

Injectable Almazine can be used with atropine sulfate, narcotic analgesics, other parenterally used analgesics, commonly used anesthetics, and muscle relaxants.

Immediately prior to intravenous use, Almazine Injection must be diluted with an equal volume of compatible solution. Contents should be mixed thoroughly by gently inverting the container repeatedly until a homogenous solution results. Do not shake vigorously, as this will result in air entrapment. When properly diluted, the drug may be injected directly into a vein or into the tubing of an existing intravenous infusion. The rate of injection should not exceed 2.0 mg per minute.

Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit. Do not use if solution is discolored or contains a precipitate.

Almazine Injection is compatible for dilution purposes with the following solutions: Sterile Water for Injection, USP; Sodium Chloride Injection, USP; 5% Dextrose Injection, USP.


Seek emergency medical attention or call the Poison Help line at 1-800-222-1222. An overdose of lorazepam can be fatal if you take it with alcohol, opioid medicine, or other drugs that cause drowsiness or slow your breathing.

Overdose symptoms may include extreme drowsiness, confusion, slurred speech, feeling restless, muscle weakness, loss of balance or coordination, feeling light-headed, slow heartbeats, weak or shallow breathing, or coma.


Store Ativan at room temperature away from moisture, heat, and light.

Keep track of the amount of medicine used from each new bottle. Almazine is a drug of abuse and you should be aware if anyone is using your medicine improperly or without a prescription.

Side effects

The most common side effects associated with Almazine are:

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Side effect occurrence does not only depend on medication you are taking, but also on your overall health and other factors.


Almazine should be avoided in people with:

Sleep apnea – Sleep apnea may be worsened by Almazine's central nervous system depressant effects. It may further reduce the patient's ability to protect his or her airway during sleep.

Myasthenia gravis – This condition is characterized by muscle weakness, so a muscle relaxant such as Almazine may exacerbate symptoms.

Pregnancy and breast feeding – Almazine belongs to the Food and Drug Administration (FDA) pregnancy category D, which means it is likely to cause harm to the developing baby, if taken during the first trimester of pregnancy. Evidence is inconclusive whether Almazine, if taken early in pregnancy, results in reduced intelligence, neurodevelopmental problems, physical malformations in cardiac or facial structure, or other malformations in some newborns. Almazine given to pregnant women antenatally may cause floppy infant syndrome in the neonate, or respiratory depression necessitating ventilation. Regular Almazine use during late pregnancy (the third trimester), carries a definite risk of benzodiazepine withdrawal syndrome in the neonate. Neonatal benzodiazepine withdrawal may include hypotonia, reluctance to suck, apneic spells, cyanosis, and impaired metabolic responses to cold stress. Symptoms of floppy infant syndrome and the neonatal benzodiazepine withdrawal syndrome have been reported to persist from hours to months after birth. Almazine may also inhibit fetal liver bilirubin glucuronidation, leading to neonatal jaundice. Almazine is present in breast milk, so caution must be exercised about breast feeding.

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In the single conditioning trial, rats were given the target taste (sucrose) and 65min later were injected with lithium. Successful transformation was achieved via somatic embryogenesis using Agrobacterium tumefaciens strain LBA4404, carrying a binary plasmid vector system containing neomycin phosphotransferase (NPT II) gene as the selectable marker and beta-glucuronidase (GUS) as a reporter gene. The effects of stimulant and depressant drugs on verbal conditioning. The results confirm the importance of descending control from supraspinal structures in mediating operantly conditioned change in H-reflex amplitude. Cerebrospinal fluid rhinorrhea secondary to small tumor invasion into the superior sagittal sinus--case report. In fact, the regional tracer distribution can be quantitatively assessed by polar map analysis if the effects of photon attenuation are accounted for.

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Lymphography in the diagnosis and treatment of cervical carcinoma. Age-dependent penetrance was estimated by the Kaplan-Meier method and compared by log-rank test. In addition, an attenuated HR response to exercise, a manifestation of chronotropic incompetence, may have independent diagnostic value for CAD. A retrospective review was performed of all patients receiving vemurafenib at Peter MacCallum Cancer Centre. For the first time it is shown in a general population study, that children as young as 1.5 years may feldene gel buy australia suffer from mental illness as older children do. Effects on antitumor activity and cytokine production in the thoracic cavity by intrapleural administration of Lactobacillus casei in tumor-bearing mice.

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The brain regulates information flow by balancing the segregation and integration of incoming stimuli to facilitate flexible cognition and behaviour. The phytoiatric antifungal activity of various derivatives of 2-iodobenzanilides. We have examined the development of expression of these substances using antibody immunocytochemistry. Peptide Immunotherapy in Vaccine Development: From Epitope to Adjuvant. Scores for patient satisfaction on the structure, process, discomfort, and general satisfaction scales of the questionnaire were used as the main outcome measures.

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Observational case series of 87 control and 73 subclinical keratoconus eyes. The same analysis applied to five germline VH genes of Heterodontus francisci shows the same result as was found with the rainbow trout. This review focuses on the purpose, considerations and methods for providing information during the preprocedural evaluation process based on the most recent literature review. Increasing age at symptom onset is strongly associated with higher occurrence of erosions within the first year unexplained by greater disease severity. Pulmonary surfactant protein A (SP-A), an alveolar glycoprotein containing collagen-like and carbohydrate recognition domains (CRD), binds P. The influence of insulin loading tests per os on insulin and glucose concentrations in blood of piglets within 40 hours from birth. Assays of 104 sera from patients with Q-fever (including index cases) using immunofluorescence for smooth muscle antibodies, microagglutination for cold agglutinins.

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