جارٍ التحقق…
تُرجمت تلقائيًا. للجرعات والتحذيرات: راجع النص الأصلي بالإنجليزية. اقرأ بالإنجليزية

Potassium

Potassium Chloride Extended-Release Tablets are indicated for the treatment and prophylaxis of hypokalemia with or without metabolic alkalosis, in pat.

ز - الأدوية التي تصرف بموجب وصفة طبية Oral Safety alerts on record

How to use Potassium

ما تقوله النشرة الرسمية. إذا وصفه لك طبيب، فاتبع الوصفة. وإذا اختلفت نشرة عبوتك، فالأولوية لها.

لمن هو

Potassium Chloride Extended-Release Tablets are indicated for the treatment and prophylaxis of hypokalemia with or without metabolic alkalosis, in patients for whom dietary management with potassium-rich foods or diuretic dose reduction is insufficient. Potassium Chloride Extended-Release Tablets are a potassium salt, indicated for the treatment and prophylaxis of hypokalemia with or without metabolic alkalosis in patients for whom dietary management with potassium-rich foods or diuretic dose reduction is insufficient. (1)

كيف يُتناول وكم مرة
  • Monitor serum potassium and adjust dosages accordingly If serum potassium is less than 2.5 mEq/L, use intravenous potassium instead of oral supplementation
  • Take with meals and with a glass of water or other liquid
  • Swallow tablets whole without crushing, chewing or sucking
  • Treatment of hypokalemia : Doses range from 40 to 100 mEq/day in divided doses
  • Limit doses to 40 mEq per dose
  • Prevention of hypokalemia : Typical dose is 20 mEq per day
  • Administration and Monitoring If serum potassium concentration is less than 2.5 mEq/L, use intravenous potassium instead of oral supplementation
  • Monitoring Monitor serum potassium and adjust dosages accordingly
  • Monitor serum potassium periodically during maintenance therapy to ensure potassium remains in desired range
  • The treatment of potassium depletion, particularly in the presence of cardiac disease, renal disease, or acidosis, requires careful attention to acid-base balance, volume status, electrolytes, including magnesium, sodium, chloride, phosphate, and calcium, electrocardiograms, and the clinical status of the patient
  • Correct volume status, acid-base balance, and electrolyte deficits as appropriate
  • Administration Take potassium chloride extended-release tablets with meals and with a glass of water or other liquid
  • Do not take potassium chloride extended-release tablets on an empty stomach because of its potential for gastric irritation [see Warnings and Precautions ]
  • Swallow tablets whole without crushing, chewing or sucking. …
Strengths it comes in

Potassium Chloride Extended-Release Tablets, USP are supplied as: The 8 mEq (600 mg) tablets are white to off-white, round, biconvex, coated tablets, debossed with “YH” and “106” on one side, and “8” on the other side. The 10 mEq (750 mg) tablets are white to off-white, round, biconvex, coated tablets, debossed with “YH” and “105” on one side, and “10” on the other side. …

Children

Safety and effectiveness in the pediatric population have not been established.

Older adults

Clinical studies of potassium chloride extended-release tablets did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects. Other reported clinical experience has not identified differences in responses between the elderly and younger patients. …

While you are taking it
  • Inform patients to take each dose with meals and with a full glass of water or other liquid, and to not crush, chew, or suck the tablets
  • Inform patients that the wax matrix is not absorbed and is excreted in the feces; in some instances the empty matrices may be noticeable in the stool
  • Advise patients seek medical attention if tarry stools or other evidence of gastrointestinal bleeding is noticed
  • Distributed by: Epic Pharma, LLC Laurelton, NY 11413 Product of Israel
  • Revised 06/2025 ZLN036
Talk to a doctor first if
  • Potassium chloride is contraindicated in patients on triamterene and amiloride
  • Concomitant use with triamterene and amiloride
Medicines it may not mix with

Triamterene and amiloride: Concomitant use is contraindicated (7.1) Renin-angiotensin-aldosterone inhibitors: Monitor for hyperkalemia (7.2) Nonsteroidal anti-inflammatory drugs: Monitor for hyperkalemia (7.3) 7.1 Triamterene or amiloride Use with triamterene or amiloride can produce severe hyperkalemia. Concomitant use is contraindicated [see Contraindications (4) ]. 7.2 Renin-angiotensin-aldosterone Inhibitors Drugs that inhibit the renin-angiotensin-aldosterone system (RAAS) including angiotensin converting enzyme (ACE) inhibitors, angiotensin receptor blockers (ARBs), spironolactone, eplerenone, or aliskiren produce potassium retention by inhibiting aldosterone production. …

Warnings

Gastrointestinal Irritation: Take with meals (5.1) 5.1 Gastrointestinal Adverse Reactions Solid oral dosage forms of potassium chloride can produce ulcerative and/or stenotic lesions of the gastrointestinal tract, particularly if the drug maintains contact with the gastrointestinal mucosa for prolonged periods. Consider the use of liquid potassium in patients with dysphagia, swallowing disorders, or severe gastrointestinal motility disorders. If severe vomiting, abdominal pain, distention, or gastrointestinal bleeding occurs, discontinue potassium chloride extended-release tablets and consider possibility of ulceration, obstruction or perforation. …

الآثار الجانبية المحتملة

The most common adverse reactions are nausea, vomiting, flatulence, abdominal pain/discomfort and diarrhea. (6) To report SUSPECTED ADVERSE REACTIONS, contact Epic Pharma, LLC at 1-888-374-2791 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch The following adverse reactions have been identified with use of oral potassium salts. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure. The most common adverse reactions to oral potassium salts are nausea, vomiting, flatulence, abdominal pain/discomfort, and diarrhea. …

Pregnancy and breastfeeding

8.1 Pregnancy Risk Summary There are no human data related to use of potassium chloride extended-release tablets during pregnancy, and animal reproduction studies have not been conducted. Potassium supplementation that does not lead to hyperkalemia is not expected to cause fetal harm. The background risk for major birth defects and miscarriage in the indicated population is unknown. …

If you take too much

10.1 Symptoms The administration of oral potassium salts to persons with normal excretory mechanisms for potassium rarely causes serious hyperkalemia. However, if excretory mechanisms are impaired, potentially fatal hyperkalemia can result [see Contraindications and Warnings] . It is important to recognize that hyperkalemia is usually asymptomatic and may be manifested only by an increased serum potassium concentration (6.5 to 8.0 mEq/L) and characteristic electrocardiographic changes (peaking of T-waves, loss of P-wave, depression of S-T segment and prolongation of the QT interval). …

إذا نسيت جرعة

تناولها عندما تتذكر، إلا إذا اقترب موعد الجرعة التالية. عندها تخطَّ الجرعة المنسية. لا تتناول جرعتين معًا أبدًا للتعويض. راجع النشرة، فبعض الأدوية مختلفة.

From the official U.S. FDA label for this active ingredient. Your pack may have a different strength, so always read its leaflet. If a doctor prescribed it, follow the prescription. Ask a pharmacist if you are unsure. Label dated 2025-09-23.

الأسماء التجارية حول العالم

Products with Potassium as the active ingredient. Names differ between countries.

Registered products

United States (FDA)

Losartan Potassium And HydrochlorothiazideLOSARTAN POTASSIUM 100 mg/1, HYDROCHLOROTHIAZIDE 12.5 mg/1 · Tablet, Film Coated · AvKARE
NDC 42291-503Label
Losartan Potassium And HydrochlorothiazideLOSARTAN POTASSIUM 50 mg/1, HYDROCHLOROTHIAZIDE 12.5 mg/1 · Tablet, Film Coated · PD-Rx Pharmaceuticals, Inc.
NDC 43063-986Label
Losartan PotassiumLOSARTAN POTASSIUM 100 mg/1 · Tablet, Film Coated · A-S Medication Solutions
NDC 50090-4712Label
Potassium AcetatePOTASSIUM ACETATE 200 meq/100mL · Injection · Exela Pharma Sciences, LLC
NDC 51754-2004Label
E.o.l.STILLINGIA SYLVATICA ROOT 3 [hp_X]/mL, ZINC GLUCONATE 3 [hp_X]/mL, THIAMINE HYDROCHLORIDE 4 [hp_X]/mL · Spray · InLight Creation, LLC.
NDC 53405-0008Label

Nigeria (NAFDAC)

NAFDACAloteo A4-8086NAFDACMisinac B4-3099NAFDACEmzoclav A4-8986NAFDACRobafenac B4-5198NAFDACMyclav 156 B4-6039NAFDACNemedin-50 A11-0259NAFDACAlben ORS_ A11-0033NAFDACZimilat 375 A11-0497NAFDACSugam-625 mg B4-2492NAFDACMaxiclav 625 B4-3928NAFDACRapiclav-1 g A4-4489NAFDACGOZA Tablets B4-8151

Other countries: check your pack's registration number and we point you to your regulator.

Safety alerts and recalls

POTASSIUM CHLORIDE Inj., 10 mEq total in 100 mL Flexible Container, Highly concentrated 100 mEq/L, Rx Only, ICU Medical, Inc., Lake Forest, Illinois, 60045, USA, NDC# 0990-7074-26U.S. FDA Class I
29 Oct 2025 · Otsuka ICU Medical LLC · OngoingLabeling: Label Error on Declared Strength-The overwrap label may incorrectly identify the product as POTASSIUM CHLORIDE Inj. 10 mEq instead of POTASSIUM CHLORIDE Inj. 20 mEq
POTASSIUM CHLORIDE Inj., 20 mEq total in 50 mL Flexible Container, Highly concentrated 400 mEq/L, Rx Only, ICU Medical, Inc., Lake Forest, Illinois, 60045, USA, NDC# 0990-7077-14U.S. FDA Class I
29 Oct 2025 · Otsuka ICU Medical LLC · OngoingLabeling: Label Error on Declared Strength-The overwrap label may incorrectly identify the product as POTASSIUM CHLORIDE Inj. 10 mEq instead of POTASSIUM CHLORIDE Inj. 20 mEq
POTASSIUM CHLORIDE Inj., 10 mEq total in 100 mL, 100 mEq/L flexible container, Rx Only, ICU Medical, Inc., Lake Forest, Illinois, 60045, USA, NDC# 0990-7074-26; Bar Code (01)003099U.S. FDA Class I
13 Feb 2025 · ICU Medical, Inc. · OngoingLabeling: Label Error on Declared Strength. Overwrap labeled as Potassium Chloride Inj 10 mEq may contain flexible containers of Potassium Chloride Inj 20 mEq
POTASSIUM CHLORIDE Inj., 20 mEq total in 100 mL flexible container 24 x case, 200 mEq/L, Rx Only, ICU Medical, Inc., Lake Forest, Illinois, 60045, USA, NDC# 0990-7075-26; Bar Code U.S. FDA Class I
13 Feb 2025 · ICU Medical, Inc. · OngoingLabeling: Label Error on Declared Strength. Cases labeled POTASSIUM CHLORIDE 20 mEq, may contain flexible containers with overwrap mislabeled as 10 mEq. The correct dosage strength of 20 mEq is printed on the labeling affixed to the product flexible container.

A recall usually affects certain batches only. Compare the lot number on your pack.

Check your pack of Potassium

أو التقط صورًا للعبوة
تبقّت 3 عمليات تحقق مجانية اليوم المصادر الرسمية: FDA الأمريكية · EMA (الاتحاد الأوروبي) · NAFDAC · تنبيهات منظمة الصحة العالمية

Questions about Potassium

What is Potassium used for?

Potassium Chloride Extended-Release Tablets are indicated for the treatment and prophylaxis of hypokalemia with or without metabolic alkalosis, in patients for whom dietary management with potassium-rich foods or diuretic dose reduction is insufficient. Potassium Chloride Extended-Release Tablets are a potassium salt, indicated for the treatment and prophylaxis of hypokalemia with or without metabolic alkalosis in pa (From the official U.S. FDA label.)

How do I take Potassium?

Follow your prescription or the leaflet in your pack. The official label says: Monitor serum potassium and adjust dosages accordingly (2.1) If serum potassium is less than 2.5 mEq/L, use intravenous potassium instead of oral supplementation (2.1) Take with meals and with a glass of water or other liquid. Swallow tablets whole without crushing, chewing or sucking. (2.1) Treatment of hypokalemia : Doses range from 40 to 100 mEq/day in divided doses. Limit d…

Do I need a prescription for Potassium?

Usually yes. Potassium is a prescription medicine in most countries. Rules differ by country.

What brands contain Potassium?

Potassium is sold under names such as Potassium Chloride. Brand names differ between countries.

How can I check that my Potassium is genuine?

Scan the registration number on your pack with PillVera (NAFDAC number in Nigeria, NDC in the United States, DIN in Canada), check the expiry date and buy only from licensed pharmacies.