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Alzotime (Alprazolam)
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Alzotime

Alzotime is commonly used to treat anxiety and panic disorders. It falls into a category of medications called benzodiazepines. They are known to affect the central nervous system components and produce a calming effect, thus decreasing brain activity.

Other names for this medication:
Alamflu, Alprasert, Alprose, Alprosym, Altrex, Alzolite, Alzopax, Ansilumirm, Anxigon, Anxit, Anxorel, Anzocalm, Apsolam, Coolam, Cooltime, Cqlam, Depser, Emcalm, Esteem, Fluxin, Imprax, Prazil, Prazolam, Prozolam, Rozin, Sanprazole, Selamb, Somnarest, Suzilam, Tenfree, Tenscure, Tranax, Zedep, Zeecam, Zocam, Zodia, Zolorel, Zopain

Similar Products:
Ditropan, Trandate, Sumycin, Arcoxia, Cycrin, Lasix, Diovan, Anafranil, Donasure, Miten, Shwas, Resquin, Trizole, Calmnir, Valium, Asthocap, Cipro,

Also known as: Alprazolam

Description

Alzotime is a benzodiazepine (ben-zoe-dye-AZE-eh-peen). Alprazolam affects chemicals in the brain that may be unbalanced in people with anxiety. Alzotime is used to treat anxiety disorders, panic disorders, and anxiety caused by depression.

You should not use Alzotime if you have narrow-angle glaucoma, if you also take itraconazole or ketoconazole, or if you are allergic to Alzotime or similar medicines (Valium, Ativan, Tranxene, and others).

Alprazolam may be habit-forming. Misuse of habit-forming medicine can cause addiction, overdose, or death.

Do not drink alcohol while taking Alzotime. This medication can increase the effects of alcohol. Alprazolam may be habit-forming and should be used only by the person for whom it was prescribed. Keep the medication in a secure place where others cannot get to it.

Dosage

This section provides information on the proper use of a number of products that contain alprazolam. It may not be specific to Alzotime XR. Please read with care.

Take this medicine only as directed by your doctor. Do not take more of it, do not take it more often, and do not take it for a longer time than your doctor ordered. If too much of this medicine is used for a long time, it may become habit-forming (causing mental or physical dependence) or cause an overdose.

This medicine should come with a Medication Guide. Read and follow the instructions carefully. Ask your doctor if you have any questions.

Swallow the extended-release tablet or tablet whole with a full glass of water. Do not break, crush, or chew it.

If you are using the orally disintegrating tablet, make sure your hands are dry before you handle the tablet. Do not remove the tablets from the bottle until you are ready to take it. Place the tablet immediately on the top of your tongue. It should melt quickly and be swallowed with saliva.

If you are using the oral liquid, measure the dose with a marked measuring spoon, oral syringe, or medicine cup.

Do not eat grapefruit or drink grapefruit juice while you are using this medicine.

The dose of this medicine will be different for different patients. Follow your doctor's orders or the directions on the label. The following information includes only the average doses of this medicine. If your dose is different, do not change it unless your doctor tells you to do so.

The amount of medicine that you take depends on the strength of the medicine. Also, the number of doses you take each day, the time allowed between doses, and the length of time you take the medicine depend on the medical problem for which you are using the medicine.

For anxiety: For oral dosage forms (solution, tablets, or orally disintegrating tablets): Adults—At first, 0.25 to 0.5 milligram (mg) 3 times a day. Your doctor may increase your dose as needed. However, the dose is usually not more than 4 mg per day. Older adults—At first, 0.25 mg 2 or 3 times a day. Your doctor may increase your dose as needed. Children—Use and dose must be determined by your doctor. For panic disorder: For oral dosage form (extended-release tablets): Adults—At first, 0.5 to 1 milligram (mg) taken in the morning once a day. Your doctor may increase your dose as needed. However, the dose is usually not more than 10 mg per day. Older adults—At first, 0.5 mg taken in the morning once a day. Your doctor may increase your dose as needed. Children—Use and dose must be determined by your doctor. For oral dosage forms (solution, tablets, or orally disintegrating tablets): Adults—At first, 0.5 milligram (mg) 3 times a day. Your doctor may increase your dose as needed. However, the dose is usually not more than 10 mg per day. Older adults—At first, 0.25 mg 2 or 3 times a day. Your doctor may increase your dose as needed. Children—Use and dose must be determined by your doctor.

Overdose

Seek emergency medical attention if you think you have used too much of this medicine. An overdose of Alzotime XR can be fatal.

Overdose symptoms may include extreme drowsiness, confusion, muscle weakness, loss of balance or coordination, feeling light-headed, fainting, and coma.

Storage

Store the medicine in a closed container at room temperature, away from heat, moisture, and direct light. Keep from freezing.

Keep out of the reach of children.

Do not keep outdated medicine or medicine no longer needed.

Ask your healthcare professional how you should dispose of any medicine you do not use.

It is very important to protect the orally disintegrating tablets from moisture. Remove and throw away any cotton packaging from the medicine bottle when you first use the medicine.

Detailed Alzotime XR dosage information

Side effects

The most common side effects associated with Alzotime 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.

Contraindications

Avoid drinking alcohol. Dangerous side effects or death could occur.

Avoid driving or hazardous activity until you know how this medicine will affect you. Dizziness or drowsiness can cause falls, accidents, or severe injuries.

Grapefruit may interact with alprazolam and lead to unwanted side effects. Avoid the use of grapefruit products.

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Development of a macromolecular dual-modality MR-optical imaging for sentinel lymph node mapping. These results indicate that the VuNCED1 cDNA encodes a 9-cis-epoxycarotenoid dioxygenase and that its product has a key role in the synthesis of ABA under drought stress. Each had a cerebrospinal fluid pleocytosis at the initial lumbar puncture. Pegylated liposomes have potential as vehicles for intratumoral and subcutaneous drug delivery. Activation of protein kinase C inhibits hormonal stimulation of the GTPase activity of Gi in human platelets. Intriguingly, mutagenesis and pharmacological inhibitor studies suggest a role for MICAL flavoenzyme redox functions in semaphorin/plexin-mediated axonal pathfinding events. Three serovars of Salmonella choleraesuis (IIIb 61:k:1,5,(7), Enteritidis and Dublin) were grown in broths of pH 5.5 and 6.2 and incubated at 4, 6, 8 or 12 degrees C. The epidemiological features of herd infection have been sporadic incidents, with only small numbers of cattle becoming infected in the majority of incidents.

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Plasmids which express either the S1 subunit or the B oligomer were then introduced into this strain. Antiperistaltic bowel segment for prevention of ileoproctostomy diarrhea. The T4CP of conjugative plasmid R388 is TrwB, a DNA-dependent ATPase. Elbow extension may be lost during lengthening, but in the adolescent age group, full return of elbow motion can be expected. The space between two residues postulated to be involved in agonist binding, Asp-80 and Asn-390, perfectly accommodated an anti-dopamine molecule. In healthy humans, BALT can only be found in the lungs of children and adolescents. Projections of luteinizing hormone-releasing hormone and vasotocin fibers to the anterior part of the preoptic nucleus in the toad, Bufo japonicus. We have demonstrated good precision and accuracy on 6 clinical chemistry analytes, 2 enzymes, potassium and theophylline using this system.

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31P NMR spectroscopy thus appears to be a suitable technique for studying the effects of pharmacological agents and other treatments for amelioration of ischemic effects on the bowel. Characterization of the free form of murein-lipoprotein from the outer membrane of Escherichia coli B/r. A possible associated factor of NSSI in BPD may be alexithymia, which reflects difficulties in identifying and communicating feelings. Ultimately, guidelines are needed for donor screening from high-risk areas, interpretation of studies and management of infected patients to ensure safe transplantation. In addition, the exclusion of other liver processes for the differential diagnosis is possible with the angiogram. LH and FSH responses to luteinizing-releasing hormone in normal, adult, human males.

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Continuous infusion interleukin-2 and tumor-derived activated cells as treatment of advanced solid tumors: a National Biotherapy Study Group Trial. Twenty-six evaluable patients with advanced or recurrent squamous cell carcinoma of the uterine cervix were treated with mitoxantrone at a dosage of 12 mg/m2 every 3 weeks. Although S-100-protein-positive sustentacular-like cells (SCs), morphologically similar to IaDCs, were also present, these were clearly distinguished from IaDCs by our double immunostaining method. The objective was to estimate whether maternal obesity and/or obstetric interventions are associated with diagnosed maternal post-partum sepsis. The brain-in-motion study: effect of a 6-month aerobic exercise intervention on cerebrovascular regulation and cognitive function in older adults. Transcatheter aortic valve replacement is proof that cardiac specialists have embraced the endovascular revolution.

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Optimal application of high-frequency ventilation in infants: a theoretical study. In vivo DTI-derived measurements of axial diffusion differentiated between mild, moderate, and severe contusive SCI with good histological correlation. An additional objective was to compare intraoral scanners with the indirect digitization of model scanners. Chronic cerebral hypoperfusion is a major cause of age-related vascular cognitive impairment. The possible mechanisms by which each might perturb the innate immune response are reviewed in a search for potential novel pathways through which transfusion can lead to an altered inflammatory response. Individually, only FGF caused a 3.0-fold increase (P less than 0.005) in AChR aggregation, without influencing the total number of AChRs. Infectious Disease Surveillance in the Woylie (Bettongia penicillata). Exposure of exponentially growing cells to a noncytotoxic concentration (0.5 mM) of PD 128763 for 2 h immediately following X irradiation increased their radiation sensitivity, modifying both the shoulder and the slope of the survival curve. A pilot study of the combination of 5-FU and epirubicin for gastric cancer as an adjuvant chemotherapy.

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Impact of preoperative knee deformity on the outcome of total knee replacement using the PFC system. Effect of porcine follicular fluid proteins and peptides on oocyte maturation and their subsequent effect on in vitro fertilization. Some of the published trials have flaws in conception and realization: heterogeneity of material, absence of randomization, incomplete follow-up and incomplete data in results. The critically ill patient presents a pharmaceutical dilemma, with the clinical condition often necessitating the administration of potent medications. However, whether 12-deoxyphorbol 13-palmitate affects angiogenesis remains unclear. Our results show that the reduction in messenger RNA (mRNA) levels of CYP1A2, CYP2A5, and CYP3A11 during turpentine-induced inflammation was abrogated in IL-6-deficient mice, confirming that IL-6 is an indispensable player for the down-regulation of hepatic CYP during aseptic inflammation. A further increase in stimulation intensity to include activation of C fibers did not reveal any more components. Content and dynamics of the human antibody variable region repertoire to the Haemophilus influenzae type b polysaccharide. Segmental lordosis was measured on preoperative standing, intraoperative prone, and postoperative standing radiographs. All patients underwent postoperative duplex ultrasound study and clinical follow-up at 1, 6, and 12 months and every year thereafter.

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Morphological and pharmacological analysis of putative serotonergic bipolar and amacrine cells in the retina of a turtle, Pseudemys scripta elegans. The oxygenation defect and radiographic densities in mechanically ventilated patients with pulmonary dysfunction and ALI/ARDS after trauma and surgery are likely caused by plavix dosage range atelectasis rather than by increased permeability-oedema related to red cell transfusion. The relaxivities of the Gd-complexes are enhanced compared to Gd-DOTA. coli and its phages has been analysed for the frequency of occurrence of nearest neighbour base doublets and codons. Pro-inflammatory genetic profiles are significantly more common in subjects with PAOD. The pneumocolon technique in small bowel meal examination is used to obtain double-contrast views of the distal ileum. CPZ affects neutrophil funcjtion as well as other aspects of immune response. These results show that the F-DLC coating may be useful for blood-contacting devices. Two cases of dissecting aneurysm are reported in which extensive aortography failed to show evidence of dissection. Bacterial attachment to the intestine is the first step in the initiation of many intestinal infections.

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Transplanted progenitors generate functional enteric neurons in the postnatal colon. We present the crystal structure of the monocot-specific EAR-2 peptide in complex with the TOPLESS-related protein 2 (TPR2) TPD, in which the EAR-2 motif binds the same TPD groove as jasmonate and auxin signaling repressors but makes additional contacts with a second TPD site to mediate TPD tetramer-tetramer interaction. Results indicated differences in pressure distribution over the first metatarsal area of the foot, in existing shoe designs. Chickens hyperimmunized with group A streptococcal vaccine often synthesize high levels of antibody to group A streptococcal carbohydrate (SACHO). The place of psychiatry in the management network of drug addicts: apropos of public psychiatry in Lausanne. The checkpoint of mitotic spindle assembly, aberrant activation of cyclin-dependent kinases, and the c-Jun N-terminal kinase/stress-activated protein kinase (JNK/SAPK) are shown to be involved in paclitaxel-induced apoptosis. administration of cisplatin and any of the sulfur-containing nucleophiles leads to a significant protection against the nephrotoxicity but reduced the anti-neoplastic activity of cisplatin when measured against the Walker 256 carcinosarcoma. The SAHD appears to be a reliable and valid measure of desire for death among terminally ill cancer patients. Clone 9 provides a novel model for further investigation of the mechanism of anti-oestrogen resistance that occurs without loss of oestrogen receptors.

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BALB/c mice were depleted of B cells by anti-mu treatment to investigate the pathogenesis of respiratory syncytial virus (RSV) infection in the absence of antibody. Integrin alphavbeta6 co-localized in the same area as TN-C and TN-C(L) immunoreactivity at the cell-cell contacts of the basal and suprabasal cell layers of the wound epithelium. Thus, the current results indicated that caveolin-1 expression may have potential both as a diagnostic marker in the differential diagnosis of renal tumors and as a therapeutic target, especially for CCRCC. The chest X-ray films revealed an anterior mediastinal mass shadow. Fas expression on freshly isolated lymphocytes was evaluated by means of immunofluorescence using polyclonal rabbit anti-Fas IgG antibody. Our results suggest that the tDCS technique showed small trends on postmenopausal vasomotor symptoms, justifying searches for more effective methods by which tDCS could reduce hot flashes. For the characterization of atherosclerotic disease in human aortic specimens two indices of ultrasonic signal loss have been developed. After 5 cycles of therapy, no evidence of graft rejection has been observed to date, and the patient achieved a complete remission, and is currently off therapy.

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