Indapamide does not affect the alertness or directly to driving itself, but can produce certain reactions in specific cases dizziness, fatigue or weakness due to the reduction in blood pressure, especially at the beginning of treatment or when added another antihypertensive agent. Ask your doctor to explain any aspect that you do not understand, contained in the instruction leaflet that comes with the medicine. Besides the active ingredient, the tablets may include lactose, corn starch, magnesium stearate, polyvidone, talc, titanium dioxide, sodium lauryl sulfate, white beeswax, glycerol, macrogolmethylcellulose, croscarmellose sodium, polyethylene glycol and coloring agents.
There is hypervolemia during normal pregnancy which is not harmful to either the fetus or the mother in the absence of cardiovascular diseasebut which is associated with edema, including generalized edema in the majority of pregnant women. Pms-Indapamide Tablet works by increasing urine production from kidneys to lower blood pressure.
If the response to 2. There are, however, no adequate and well controlled studies in pregnant women.
Your doctor can check before starting treatment the level of potassium and calcium in the blood, doing this also repeatedly during the course of treatment. An evacuation of the stomach is recommended by emesis and gastric lavage after which the electrolyte and fluid balance should be evaluated carefully.
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The side effects listed below are not experienced by everyone who takes this medication. The usual dose is one tablet a day, preferably in the morning. The safety and effectiveness of indapamide for use by children have not been established.
The contents herein are for informational purposes only. Consult your doctor if you observe any of the following side-effects, especially if they do not go away. Interference with adequate oral intake of electrolytes will also contribute to hypokalemia. If you are taking medication for abnormal heart rhythms, discuss with your doctor how this medication may affect your medical condition, how your medical condition may affect the dosing and effectiveness of this medication, and whether any special monitoring is needed.
Warning signs include dry mouth, thirst, weakness, fatigue, lethargy, drowsiness, restlessness, muscle pains or cramps, hypotension, oliguria, tachycardia, and gastrointestinal disturbance. After 4 to 8 weeks, your doctor may increase this to 2.
There is minimal clinical trial experience in patients with doses greater than 5 mg once a day. Serum concentrations of uric acid increased by an average of 0.
Do not give this medication to anyone else, even if they have the same symptoms as you do. If you have liver disease or reduced liver function, discuss with your doctor how this medication may affect your medical condition, how your medical condition may affect the dosing and effectiveness of this medication, and whether any special monitoring is needed.
The contents of this site are for informational purposes only and are meant to be discussed with your physician or other qualified health care professional before being acted on. If you are concerned about side effects, discuss the risks and benefits of this medication with your doctor. Contact your doctor at once if you experience signs of an allergic reaction, such as skin rash, itching, difficulty breathing or swelling of the face and throat.
If you are taking medication for abnormal heart rhythms, discuss with your doctor how this medication may affect your medical condition, how your medical condition may affect the dosing and effectiveness of this medication, and whether any special monitoring is needed. How to dispose of unused medications - Accessed: ShowAd "x90", "bottomadDesktop", "2", 12, false, bottomadDesktopMapping .