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Theocort (Theophylline)

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Theocort is a bronchodilator. This drug is used to treat asthma and COPD, like chronic bronchitis or emphysema. It opens the airways in the lungs so it is easier to breathe. Theocort is a long-term medication that helps you breathe easier when you have asthma or COPD, but it is not a first-choice medication for these problems.

Other names for this medication:
Airomol, Alergin, Ambrolax, Ambrolite, Asmasule, Asmatide, Asthasol, Asthimo, Asthmino, Asthocap, Biodryl, Bronchophyl, Broncure, Bronkese, Carbasma, Duralyn, Durasalyn, Elixophyllin, Lontif, Mediphylline, Mucoresp, Mucorespules, Onimar, Phylobid, Phyloday, Quibron, Relasmin, Salbeto, Salphylline, Solbeta, Solebeta, Sphylin, Theobric, Theoclear, Theocort, Theofil, Theophylline, Theoriv, Theostan, Theotabllin, Theotas, Thiosol, Unicontin, Ventil, Ventirex, Zeriphyllin, Zeriphylline

Similar Products:
Lunesta, Kemadrin, Viagra, Seroquel, Maxalt, Suprax, Pepcid, Theolair

Also known as: Theophylline


Valtrex (valacyclovir) is an antiviral drug. It slows the growth and spread of the herpes virus to help the body fight the infection.

Valtrex is used to treat infections caused by herpes viruses, including genital herpes, cold sores, and shingles (herpes zoster) in adults.

Valtrex is used to treat cold sores in children who are at least 12 years old, or chickenpox in children who are at least 2 years old.

Valtrex will not cure herpes and will not prevent you from spreading the virus to other people. However, this medicine can lessen the symptoms of an infection.


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

In addition to the use of this medicine, treatment for your high blood pressure may include weight control and changes in the types of foods you eat, especially foods high in sodium. Your doctor will tell you which of these are most important for you. You should check with your doctor before changing your diet .

Many patients who have high blood pressure will not notice any signs of the problem. In fact, many may feel normal. It is very important that you take your medicine exactly as directed and that you keep your appointments with your doctor even if you feel well .

Remember that this medicine will not cure your high blood pressure, but it does help control it. You must continue to take it as directed if you expect to lower your blood pressure and keep it down. You may have to take high blood pressure medicine for the rest of your life. If high blood pressure is not treated, it can cause serious problems such as heart failure, blood vessel disease, stroke, or kidney disease .

Swallow the extended-release tablet whole with a full glass of water. Do not break, crush, or chew it. It is best to take this medicine with food .

If you cannot swallow the verapamil extended-release capsules, you may open it and sprinkle the pellets contained in the capsule on one tablespoon of applesauce. This mixture must be swallowed immediately with a glass of cool water. The applesauce should not be hot and should be soft enough to be swallowed without chewing. Do not chew or crush the pellets .

If you are taking the extended-release tablets, you may sometimes notice what looks like a tablet in your stool. This is the empty tablet shell that is left after the medicine has been absorbed .

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 chest pain: For oral dosage form (tablets): Adults—The usual dose is 80 to 120 milligrams (mg) three times a day. Your doctor may adjust your dose if needed. Children—Use and dose must be determined by your doctor . For oral dosage form (extended-release tablets, 24 hr): Adults—At first, 180 milligrams (mg) once daily at bedtime. Your doctor may adjust your dose if needed. Children—Use and dose must be determined by your doctor . For heart rhythm problems: For oral dosage form (tablets): Adults—The total usual dose is 240 to 480 milligrams (mg) divided in three or four equal doses per day. Children—Use and dose must be determined by your doctor . For high blood pressure: For oral dosage form (tablets): Adults—At first, 80 milligrams (mg) three times a day. Your doctor may adjust your dose if needed. Children—Use and dose must be determined by your doctor . For oral dosage form (extended-release capsules): Adults—At first, 200 milligrams (mg) once daily at bedtime. Your doctor may adjust your dose if needed. Children—Use and dose must be determined by your doctor . For oral dosage form (extended-release tablets): Adults—At first, 180 milligrams (mg) once daily in the morning. Your doctor may adjust your dose if needed. Children—Use and dose must be determined by your doctor . For oral dosage form (extended-release tablets, 24 hr): Adults—At first, 180 milligrams (mg) once daily at bedtime. Your doctor may adjust your dose if needed. Children—Use and dose must be determined by your doctor .


If you overdose Generic Theocort and you don't feel good you should visit your doctor or health care provider immediately.


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.

Detailed Abilify MyCite dosage information

Side effects

The most common side effects associated with Theocort 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.


If you are breastfeeding, the chance that problems might occur depends on the ingredients of the combination. For the individual ingredients of these combinations, the following apply:

Acetaminophen—Acetaminophen passes into the breast milk. However, it has not been reported to cause problems in nursing babies. Alcohol—Alcohol passes into the breast milk. However, the amount of alcohol in recommended doses of this medicine does not usually cause problems in nursing babies. Antihistamines—Small amounts of antihistamines pass into the breast milk. Antihistamine-containing medicine is not recommended for use while breastfeeding since most antihistamines are especially likely to cause side effects, such as unusual excitement or irritability, in the baby. Also, since antihistamines tend to decrease the secretions of the body, the flow of breast milk may be reduced in some patients. Caffeine—Small amounts of caffeine pass into the breast milk and may build up in the nursing baby. However, the amount of caffeine in recommended doses of this medicine does not usually cause problems in nursing babies. Codeine and other narcotic cough medicines (e.g., dihydrocodeine, hydrocodone, and hydromorphone)—Codeine is changed to morphine in the body. Some people change codeine to morphine more quickly than others. These individuals are called "ultra-rapid metabolizers of codeine". If a nursing mother is an ultra-rapid metabolizer of codeine, it could lead to a morphine overdose in the nursing baby and cause very serious side effects. A nursing mother should talk to her doctor if she has any questions about taking codeine or about how this medicine may affect her baby . Decongestants (e.g., ephedrine, phenylephrine, pseudoephedrine—Phenylephrine has not been reported to cause problems in nursing babies. Ephedrine and pseudoephedrine pass into the breast milk and may cause unwanted effects in nursing babies (especially newborn and premature babies). Iodides (e.g., calcium iodide and iodinated glycerol)—These medicines pass into the breast milk and may cause unwanted effects, such as underactive thyroid, in the baby. Salicylates (e.g., aspirin)—Salicylates pass into the breast milk. Although salicylates have not been reported to cause problems in nursing babies, it is possible that problems may occur if large amounts are taken regularly.

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A-PE- and S-PE-liposomes evoke, after intravenous injection in mice, a humoral response. The aim of this study was to monitor exposure to heavy metal contaminants from habitual diets and to estimate the health risk for the consumer by comparing the analyzed content with the acceptable daily intake (ADI). The excretion of 18-oxocortisol increased from an average of 3.7 nmol/day to a peak of 176.7 nmol/day (a 47-fold increase) on the third day and decreased to 107.9 nmol/day on the fifth day of ACTH administration. Fluorometric determination of sub-nanogram levels of nitrite using 5-aminofluorescein. Our experience with the operation of a central sterilization unit. Vice versa, benzodiazepines or anxiolytic beta-carbolines (ZK 93423, 10(-5) M) added to membranes from naive rats increase GABA binding to the level of unstressed rats and remove the decrease in the density of GABA receptors elicited by anxiogenic beta-carbolines. coli were attenuated in cPLA(2)-alpha(-/-) mice compared with wild type littermates. Applications of magnetic resonance techniques to deep tumor hyperthermia.

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Fluorescence microscopy of sections of the cord show that the fluorescence leaves the subarachnoid space at the point where the spinal nerves traverse the arachnoid membrane. 9-Aminoacridine mutagenesis of bacteriophage T4 intracellular DNA. Effect of 51p1-related gene copy number (V1-69 locus) on production of hepatitis C-associated cryoglobulins. The aim of this paper is to highlight the relationship between HIV infection and acquired rectal fistula (RF) in children in order to create awareness among clinicians who attend to children. Aneurysm of a pulmonary artery branch: an uncommon cause of a coin lesion. The determination of urinary estrogens in pregnancy using an automated fluorometric assay. The ability of the tyrosine kinase inhibitor sunitinib to enhance immunotherapy in the setting of HCC was evaluated. Methodological studies related to cardiovascular risk assessment.

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Practice variations and health care reform: connecting the dots. No guidelines exist for the evaluation of patients after near hanging. Transient expression of exogenous MyoD1 in these cells is sufficient to activate endogenous MLC 1 and cardiac alpha-actin mRNA synthesis during muscle differentiation. Diazepam was considered to offer greater reliability and ease of administration. Using a cotransfection assay, we found that hGATA-1 can efficiently activate transcription of the -95 GPB construct in non-erythroid cells. Protection by acetalization of the 24-oxo-group of these methyl esters with ethylene glycol, followed by alkaline hydrolysis, gave 3alpha,7alpha,12alpha-trihydroxy- and 3alpha,7alpha-dihydroxy-24,24-ethylenedioxy-5beta-cholestan-26-oic acids. It is shown herein that, on both theoretical and experimental grounds, significant contribution to hydrolysis by high affinity PDE activity would lead to striking departures from proportionality of the relationships between rates of cAMP synthesis and intracellular cAMP accumulations. In this work, we present spectroscopic data that provide insight into the ligation of the heme iron in the soluble domain of CcmE from Escherichia coli.


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Thyrotrophin response to thyrotrophin-releasing hormone in unipolar and bipolar affective illness. Soy greases with lithium-fatty acid soap having C12-C18 chain lengths and different metal to fatty acid ratios were synthesized. This study provides the first report on in vivo replication of a recombinant norovirus strain isolated following in vitro coinfection. ODCs and postmigrating precursors contained in P13 normal corpus callosum survived, migrated out of the graft and myelinated in the shi host generic xanax pictures mg parenchyma. These results indicate that the secretion of lysosomal enzymes into pancreatic juice is stimulated by gut hormones, such as caerulein, in the normal physiological state and in pathological states, such as PDO. In three adult macaques the retrograde degeneration of cell bodies in the motor cortex was investigated 6 months after unilateral pyramidal tract section.

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Complications of the early postoperative period in craniocerebral injuries and ways of preventing them. The feedback control depends upon the activity of the cAMP-dependent protein kinases and requires the presence of the CDC25 and RAS proteins. This study reveals molecular genetic mechanisms underlying a role for mitochondria in carcinogenesis in humans. Here, Margaret Kidwell and Jose Ribeiro develop a rationale for the possible use of transposable genetic elements, one of these potential drive mechanisms, and some of the problems being faced in seeking to determine the feasibility of such a strategy are described. Independent of the level of motor activity, higher or lower than the control groups, habituation still occurs following DA agonists (amphetamine and apomorphine) and antagonist (chlorpromazine) injections in rats submitted to the open field test. Epileptiform discharges and behavioral seizures may be the consequences of excess excitation from inadequate inhibitory effects associated with gamma-aminobutyric acid (GABA).

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The use of species-specific antibodies directed against mouse endothelial cells demonstrated the respective participation of the host and the donor in the formation of new vessels in the graft after crossed rabbit into mouse and mouse into rat transplantation experiments. Combing sonic technology with hand instrumentation facilitates root canal preparation. At various intervals from day 0 to day 180 following operation the mechanical characteristics of the bone were evaluated. Filamentous blastocysts appeared to have less P450(17) alpha) protein than did littermate tubular blastocysts. The D4 receptor antagonist, clozapine, translated paired-pulse inhibition into paired-pulse potentiation in both perforant path targets.

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Feeding ovalbumin over a wide range of doses is known to reduce subsequent systemic immune responses to parenteral immunization. Different chemokine receptors have been suggested to play a pivotal role in allergic diseases and therefore to be relevant for the activation of effector cells and propagation of the inflammatory response. The literature is reviewed, and the differential diagnosis is discussed. The biophysical activity of purified recombinant Hib porin was identical to porin isolated from the bacterial outer membrane. Frequently during the process of data analysis in epidemiological studies, the scale of one or more continuous variables is changed. It is suggested that fluctuations of tramadol dosing medscape reproduction of unstable reflexes and of efficiency of additional learning sessions depend on changes in spatial relations of bioelectrical processes in the cortex which accompany the additional learning. We have studied 57 clinical samples of 49 patients using PCR and culture in conventional media. When and how to use angiotensin-converting enzyme inhibition in congestive heart failure.

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