Losartan + Hidroclorotiazida Aurobindo Side effects

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What are the possible side effects of Losartan + Hidroclorotiazida Aurobindo?

Get emergency medical help if you have any signs of an allergic reaction to Losartan + Hidroclorotiazida Aurobindo: hives; difficulty breathing; swelling of your face, lips, tongue, or throat.

In rare cases, Losartan + Hidroclorotiazida Aurobindo can cause a condition that results in the breakdown of skeletal muscle tissue, leading to kidney failure. Call your doctor right away if you have unexplained muscle pain, tenderness, or weakness especially if you also have fever, unusual tiredness, and dark colored urine.

Call your doctor at once if you have:

Common Losartan + Hidroclorotiazida Aurobindo side effects may include:

This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

Side effects of Losartan + Hidroclorotiazida Aurobindo in details

Clinical Trials Experience

Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.

Losartan (Losartan + Hidroclorotiazida Aurobindo) potassium-Hydrochlorothiazide (Losartan (Losartan + Hidroclorotiazida Aurobindo) + Hidroclorotiazida Aurobindo) has been evaluated for safety in 858 patients treated for essential hypertension and 3889 patients treated for hypertension and left ventricular hypertrophy. Most adverse reactions have been mild and transient in nature and have not required discontinuation of therapy. In controlled clinical trials, discontinuation of therapy due to clinical adverse events was required in only 2.8% and 2.3% of patients treated with the combination and placebo, respectively.

In these double-blind controlled clinical trials, adverse reactions occurring in greater than 2% of subjects treated with Losartan (Losartan + Hidroclorotiazida Aurobindo)-Hydrochlorothiazide (Losartan (Losartan + Hidroclorotiazida Aurobindo) + Hidroclorotiazida Aurobindo) and at a greater rate than placebo were: back pain (2.1% vs 0.6%), dizziness (5.7% vs 2.9%), and upper respiratory infection (6.1% vs 4.6%).

The following additional adverse reactions have been reported in clinical trials with Losartan + Hidroclorotiazida Aurobindo and/or the individual components:

Blood and the lymphatic system disorders: Anemia, aplastic anemia, hemolytic anemia, leukopenia, agranulocytosis.

Metabolism and nutrition disorders: Anorexia, hyperglycemia, hyperuricemia, electrolyte imbalance including hyponatremia and hypokalemia.

Psychiatric disorders: Insomnia, restlessness.

Nervous system disorders: Dysgeusia, headache, migraine, paraesthesias.

Eye disorders: Xanthopsia, transient blurred vision.

Cardiac disorders: Palpitation, tachycardia.

Vascular disorders: Dose-related orthostatic effects, necrotizing angiitis (vasculitis, cutaneous vasculitis).

Respiratory, thoracic and mediastinal disorders: Nasal congestion, pharyngitis, sinus disorder, respiratory distress (including pneumonitis and pulmonary edema).

Gastrointestinal disorders: Dyspepsia, abdominal pain, gastric irritation, cramping, diarrhea, constipation, nausea, vomiting, pancreatitis, sialoadenitis.

Hepato-biliary disorders: Jaundice (intrahepatic cholestatic jaundice).

Skin and subcutaneous tissue disorders: Rash, pruritus, purpura, toxic epidermal necrolysis, urticaria, photosensitivity, cutaneous lupus erythematosus.

Musculoskeletal and connective tissue disorders: Muscle cramps, muscle spasm, myalgia, arthralgia.

Renal and urinary disorders: Glycosuria, renal dysfunction, interstitial nephritis, renal failure.

Reproductive system and breast disorders: Erectile dysfunction/impotence.

General disorders and administration site conditions: Chest pain, edema/swelling, malaise, fever, weakness.

Investigations: Liver function abnormalities.

Cough

Persistent dry cough has been associated with ACE-inhibitor use and in practice can be a cause of discontinuation of ACE-inhibitor therapy. Two prospective, parallel-group, double-blind, randomized, controlled trials were conducted to assess the effects of Losartan (Losartan + Hidroclorotiazida Aurobindo) on the incidence of cough in hypertensive patients who had experienced cough while receiving ACE-inhibitor therapy. Patients who had typical ACE-inhibitor cough when challenged with lisinopril, whose cough disappeared on placebo, were randomized to Losartan (Losartan + Hidroclorotiazida Aurobindo) 50 mg, lisinopril 20 mg, or either placebo (one study, n=97) or 25 mg Hydrochlorothiazide (Losartan (Losartan + Hidroclorotiazida Aurobindo) + Hidroclorotiazida Aurobindo) (n=135). The double-blind treatment period lasted up to 8 weeks. The incidence of cough is shown in Table 1 below.

Table 1:
*
Demographics = (89% Caucasian, 64% female)
Demographics = (90% Caucasian, 51% female)
Study 1* HCTZ Losartan (Losartan + Hidroclorotiazida Aurobindo) Lisinopril
Cough 25% 17% 69%
Study 2† Placebo Losartan (Losartan + Hidroclorotiazida Aurobindo) Lisinopril
Cough 35% 29% 62%

These studies demonstrate that the incidence of cough associated with Losartan (Losartan + Hidroclorotiazida Aurobindo) therapy, in a population that all had cough associated with ACE-inhibitor therapy, is similar to that associated with Hydrochlorothiazide (Losartan (Losartan + Hidroclorotiazida Aurobindo) + Hidroclorotiazida Aurobindo) or placebo therapy.

Cases of cough, including positive re-challenges, have been reported with the use of Losartan (Losartan + Hidroclorotiazida Aurobindo) in postmarketing experience.

Postmarketing Experience

The following adverse reactions have been identified during post-approval use of Losartan + Hidroclorotiazida Aurobindo. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to estimate their frequency reliably or to establish a causal relationship to drug exposure.

Digestive: Hepatitis has been reported rarely in patients treated with Losartan (Losartan + Hidroclorotiazida Aurobindo).

Hematologic: Thrombocytopenia.

Hypersensitivity: Angioedema, including swelling of the larynx and glottis, causing airway obstruction and/or swelling of the face, lips, pharynx, and/or tongue has been reported rarely in patients treated with Losartan (Losartan + Hidroclorotiazida Aurobindo); some of these patients previously experienced angioedema with other drugs including ACE inhibitors. Vasculitis, including Henoch-Schönlein purpura, has been reported with Losartan (Losartan + Hidroclorotiazida Aurobindo). Anaphylactic reactions have been reported.

Musculoskeletal: rhabdomyolysis

Skin: Erythroderma

What is the most important information I should know about Losartan + Hidroclorotiazida Aurobindo?

Losartan + Hidroclorotiazida Aurobindo contraindications

Hypersensitivity to Losartan (Losartan + Hidroclorotiazida Aurobindo), sulphonamide-derived substances (as Hydrochlorothiazide (Losartan (Losartan + Hidroclorotiazida Aurobindo) + Hidroclorotiazida Aurobindo)) or to any of the excipients of Losartan + Hidroclorotiazida Aurobindo.

Therapy resistant hypokalemia or hypercalcemia; severe hepatic impairment; cholestasis and biliary obstructive disorders; refractory hyponatremia; symptomatic hyperuricemia/gout; 2nd and 3rd trimester of pregnancy; lactation; severe renal impairment (ie, creatinine clearance <30 mL/min); anuria.

Excipient: Patients with rare hereditary problems of galactose intolerance, the Lapp lactase deficiency or glucose-galactose malabsorption should not take Losartan + Hidroclorotiazida Aurobindo.

Use in lactation: It is not known whether Losartan (Losartan + Hidroclorotiazida Aurobindo) is excreted in human milk. However, Losartan (Losartan + Hidroclorotiazida Aurobindo) is excreted in the milk of lactating rats. Because no information is available regarding the use of Losartan (Losartan + Hidroclorotiazida Aurobindo) during breastfeeding, Losartan (Losartan + Hidroclorotiazida Aurobindo) is not recommended and alternative treatments with better established safety profiles during breastfeeding are preferable, especially while nursing a newborn or preterm infant.

Thiazides pass into human milk and may inhibit lactation. Because of the potential for adverse effects on the nursing infant, Losartan (Losartan + Hidroclorotiazida Aurobindo)/HCTZ is contraindicated during breastfeeding.

References

  1. DailyMed. "AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL: DailyMed provides trustworthy information about marketed drugs in the United States. DailyMed is the official provider of FDA label information (package inserts).". https://dailymed.nlm.nih.gov/dailyme... (accessed September 17, 2018).
  2. DailyMed. "LOSARTAN POTASSIUM: DailyMed provides trustworthy information about marketed drugs in the United States. DailyMed is the official provider of FDA label information (package inserts).". https://dailymed.nlm.nih.gov/dailyme... (accessed September 17, 2018).
  3. DTP/NCI. "losartan: The NCI Development Therapeutics Program (DTP) provides services and resources to the academic and private-sector research communities worldwide to facilitate the discovery and development of new cancer therapeutic agents.". https://dtp.cancer.gov/dtpstandard/s... (accessed September 17, 2018).

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