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Does Plendil (felodipine) cause side effects?
Plendil (felodipine) is an oral calcium channel blocker (CCB) of the dihydropyridine (DHP) class used to treat high blood pressure to prevent heart attacks and strokes. It may be used alone or in combination with other drugs. It also is used to treat patients with angina although it is not FDA approved for this use.
Calcium is necessary for muscle cells to contract. Plendil prevents calcium from being released within the muscle cells of the small arteries and thereby causes the muscles to relax and the arteries to dilate or expand. Dilation of arteries reduces blood pressure. It has little or no effect on the muscles of veins or the heart.
Common side effects of Plendil include
Serious side effects of Plendil include
- overgrowth of gums,
- frequent urination,
- skin eruptions,
- upper respiratory tract reactions, and
Drug interactions of Plendil include cimetidine, ketoconazole, itraconazole, and erythromycin, which can block the breakdown of Plendil, resulting in higher blood concentrations of Plendil and drops in blood pressure.
- Carbamazepine, phenobarbital, or phenytoin can lower Plendil blood concentrations.
- Therefore, higher doses of f Plendil may be necessary in patients receiving these medications.
- Taking Plendil with grapefruit juice increases its absorption and may lead to sudden drops in blood pressure.
- Plendil may increase blood concentrations of tacrolimus.
- Tacrolimus blood concentrations should be monitored and the dose should be modified as necessary.
There are no adequate studies on the effects of Plendil in pregnant women. A doctor or health care professional must weigh the potential risks to the fetus against the potential benefits to the mother.
What are the important side effects of Plendil (felodipine)?
The most common side effects reported by patients include:
- Peripheral edema (swollen ankles and feet)
- Increased heart rate
- Low blood pressure
Other important side effects include:
Plendil (felodipine) side effects list for healthcare professionals
In controlled studies in the United States and overseas, approximately 3000 patients were treated with felodipine as either the extended-release or the immediate-release formulation.
The most common clinical adverse events reported with Plendil administered as monotherapy at the recommended dosage range of 2.5 mg to 10 mg once a day were peripheral edema and headache. Peripheral edema was generally mild, but it was age and dose related and resulted in discontinuation of therapy in about 3% of the enrolled patients. Discontinuation of therapy due to any clinical adverse event occurred in about 6% of the patients receiving Plendil, principally for peripheral edema, headache, or flushing.
- Adverse events that occurred with an incidence of 1.5% or greater at any of the recommended doses of 2.5 mg to 10 mg once a day (Plendil, N = 861; Placebo, N = 334), without regard to causality, are compared to placebo and are listed by dose in the table below.
- These events are reported from controlled clinical trials with patients who were randomized to a fixed dose of Plendil or titrated from an initial dose of 2.5 mg or 5 mg once a day.
- A dose of 20 mg once a day has been evaluated in some clinical studies.
- Although the antihypertensive effect of Plendil is increased at 20 mg once a day, there is a disproportionate increase in adverse events, especially those associated with vasodilatory effects.
Percent of Patients with Adverse Events in Controlled Trials* of
Plendil (N=861) as Monotherapy without Regard to Causality (Incidence of
discontinuations shown in parentheses)
|Body System Adverse Events||Placebo
|Body as a Whole|
|Peripheral Edema||3.3 (0.0)||2.0 (0.0)||8.8 (2.2)||17.4 (2.5)|
|Asthenia||3.3 (0.0)||3.9 (0.0)||3.3 (0.0)||2.2 (0.0)|
|Warm Sensation||0.0 (0.0)||0.0 (0.0)||0.9 (0.2)||1.5 (0.0)|
|Palpitation||2.4 (0.0)||0.4 (0.0)||1.4 (0.3)||2.5 (0.5)|
|Nausea||1.5 (0.9)||1.2 (0.0)||1.7 (0.3)||1.0 (0.7)|
|Dyspepsia||1.2 (0.0)||3.9 (0.0)||0.7 (0.0)||0.5 (0.0)|
|Constipation||0.9 (0.0)||1.2 (0.0)||0.3 (0.0)||1.5 (0.2)|
|Headache||10.2 (0.9)||10.6 (0.4)||11.0 (1.7)||14.7 (2.0)|
|Dizziness||2.7 (0.3)||2.7 (0.0)||3.6 (0.5)||3.7 (0.5)|
|Paresthesia||1.5 (0.3)||1.6 (0.0)||1.2 (0.0)||1.2 (0.2)|
|Upper Respiratory Infection|
|Cough||0.3 (0.0)||0.8 (0.0)||1.2 (0.0)||1.7 (0.0)|
|Rhinorrhea||0.0 (0.0)||1.6 (0.0)||0.2 (0.0)||0.2 (0.0)|
|Sneezing||0.0 (0.0)||1.6 (0.0)||0.0 (0.0)||0.0 (0.0)|
|Rash||0.9 (0.0)||2.0 (0.0)||0.2 (0.0)||0.2 (0.0)|
|Flushing||0.9 (0.3)||3.9 (0.0)||5.3 (0.7)||6.9 (1.2)|
|*Patients in titration studies may have been exposed to more than one dose level of Plendil.|
Adverse events that occurred in 0.5 up to 1.5% of patients who received Plendil in all controlled clinical trials at the recommended dosage range of 2.5 mg to 10 mg once a day, and serious adverse events that occurred at a lower rate, or events reported during marketing experience (those lower rate events are in italics) are listed below.
These events are listed in order of decreasing severity within each category, and the relationship of these events to administration of Plendil is uncertain:
- Body as a Whole: Chest pain, facial edema, flu-like illness;
- Cardiovascular: Myocardial infarction, hypotension, syncope, angina pectoris, arrhythmia, tachycardia, premature beats;
- Digestive: Abdominal pain, diarrhea, vomiting, dry mouth, flatulence, acid regurgitation;
- Endocrine: Gynecomastia;
- Hematologic: Anemia;
- Metabolic: ALT (SGPT) increased;
- Musculoskeletal: Arthralgia, back pain, leg pain, foot pain, muscle cramps, myalgia, arm pain, knee pain, hip pain;
- Nervous/Psychiatric: Insomnia, depression, anxiety disorders, irritability, nervousness, somnolence, decreased libido;
- Respiratory: Dyspnea, pharyngitis, bronchitis, influenza, sinusitis, epistaxis, respiratory infection;
- Skin: Angioedema, contusion, erythema, urticaria, leukocytoclastic vasculitis;
- Special Senses: Visual disturbances;
- Urogenital: Impotence, urinary frequency, urinary urgency, dysuria, polyuria.
- Gingival hyperplasia, usually mild, occurred in < 0.5% of patients in controlled studies. This condition may be avoided or may regress with improved dental hygiene.
Clinical Laboratory Test Findings
- No significant effects on serum electrolytes were observed during short- and long-term therapy.
- No significant effects on fasting serum glucose were observed in patients treated with Plendil in the U.S. controlled study.
- 1 of 2 episodes of elevated serum transaminases decreased once drug was discontinued in clinical studies; no follow-up was available for the other patient.
What drugs interact with Plendil (felodipine)?
Felodipine is metabolized by CYP3A4. Co-administration of CYP3A4 inhibitors (eg, ketoconazole, itraconazole, erythromycin, grapefruit juice, cimetidine) with felodipine may lead to several-fold increases in the plasma levels of felodipine, either due to an increase in bioavailability or due to a decrease in metabolism.
- These increases in concentration may lead to increased effects, (lower blood pressure and increased heart rate).
- These effects have been observed with co-administration of itraconazole (a potent CYP3A4 inhibitor). Caution should be used when CYP3A4 inhibitors are co-administered with felodipine.
A conservative approach to dosing felodipine should be taken. The following specific interactions have been reported:
- Co-administration of another extended release formulation of felodipine with itraconazole resulted in approximately 8-fold increase in the AUC, more than 6-fold increase in the Cmax, and 2-fold prolongation in the half-life of felodipine.
- Co-administration of felodipine (Plendil) with erythromycin resulted in approximately 2.5-fold increase in the AUC and Cmax, and about 2-fold prolongation in the half-life of felodipine.
- Co-administration of felodipine with grapefruit juice resulted in more than 2fold increase in the AUC and Cmax, but no prolongation in the half-life of felodipine.
- Co-administration of felodipine with cimetidine (a non-specific CYP-450 inhibitor) resulted in an increase of approximately 50% in the AUC and the Cmax, of felodipine.
- A pharmacokinetic study of felodipine in conjunction with metoprolol demonstrated no significant effects on the pharmacokinetics of felodipine.
- The AUC and Cmax of metoprolol, however, were increased approximately 31 and 38%, respectively.
- In controlled clinical trials, however, beta blockers including metoprolol were concurrently administered with felodipine and were well tolerated.
- When given concomitantly with Plendil the pharmacokinetics of digoxin in patients with heart failure were not significantly altered.
- In a pharmacokinetic study, maximum plasma concentrations of felodipine were considerably lower in epileptic patients on long-term anticonvulsant therapy (eg, phenytoin, carbamazepine, or phenobarbital) than in healthy volunteers.
- In such patients, the mean area under the felodipine plasma concentration-time curve was also reduced to approximately 6% of that observed in healthy volunteers.
- Since a clinically significant interaction may be anticipated, alternative antihypertensive therapy should be considered in these patients.
- Felodipine may increase the blood concentration of tacrolimus.
- When given concomitantly with felodipine, the tacrolimus blood concentration should be followed and the tacrolimus dose may need to be adjusted.
Other Concomitant Therapy
- In healthy subjects there were no clinically significant interactions when felodipine was given concomitantly with indomethacin or spironolactone.
Interaction with Food
- See prescribing information.
Plendil (felodipine) is an oral calcium channel blocker (CCB) of the dihydropyridine (DHP) class used to treat high blood pressure to prevent heart attacks and strokes. Common side effects of Plendil include swollen ankles and feet, headache, flushing, dizziness, increased heart rate, and low blood pressure. There are no adequate studies on the effects of Plendil in pregnant women. It is unknown if Plendil is excreted in breast milk.
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Second Source WebMD Medical Reference
High Blood Pressure (Hypertension)
High blood pressure (hypertension) is a disease in which pressure within the arteries of the body is elevated. About 75 million people in the US have hypertension (1 in 3 adults), and only half of them are able to manage it. Many people do not know that they have high blood pressure because it often has no has no warning signs or symptoms. Systolic and diastolic are the two readings in which blood pressure is measured. The American College of Cardiology released new guidelines for high blood pressure in 2017. The guidelines now state that blood normal blood pressure is 120/80 mmHg. If either one of those numbers is higher, you have high blood pressure. The American Academy of Cardiology defines high blood pressure slightly differently. The AAC considers 130/80 mm Hg. or greater (either number) stage 1 hypertension. Stage 2 hypertension is considered 140/90 mm Hg. or greater. If you have high blood pressure you are at risk of developing life threatening diseases like stroke and heart attack.REFERENCE: CDC. High Blood Pressure. Updated: Nov 13, 2017.
Pulmonary hypertension is elevated pressure in the pulmonary arteries that carry blood from the lungs to the heart. The most common symptoms are fatigue and difficulty breathing. If the condition goes undiagnosed, more severe symptoms may occur. As pulmonary hypertension worsens, some people with the condition have difficulty performing any activities that require physical exertion. While there is no cure for pulmonary hypertension, it can be managed and treated with medications and supplemental oxygen to increase blood oxygen levels.
Pseudotumor Cerebri (Idiopathic Intracranial Hypertension)
Pseudotumor Cerebri (intracranial hypertension) is a condition where there is an increase in pressure of fluid surrounding the brain and spinal cord (cerebrospinal fluid or CSF) mimicing a brain tumor. The cause is unknown. The most common symptom is headache but also include eye-pain, vision loss and double vision. Pseudotumor cerebri is diagnosed with MRI or CAT scans and treated by discontinuing offending medications (if applicable), weight loss and diuretic medications. The condition can also be helped by repeated drainage of spinal fluid using the lumbar puncture.
Preeclampsia (Pregnancy Induced Hypertension)
Preeclampsia is related to increased blood pressure and protein in the mother's urine. Preeclampsia typically begins after the 20th week of pregnancy. When preeclampsia causes seizures, it is termed "eclampsia" and is the second leading cause of maternal death of in the US. Preeclampsia is the leading cause of fetal complications. Risk factors for preeclampsia include high blood pressure, obesity, multiple births, and women with preexisting medical conditions such as diabetes, kidney disease, rheumatoid arthritis, lupus, or scleroderma. Pregnancy planning and lifestyle changes may reduce the risk of preeclampsia during pregnancy.
Portal hypertension is most commonly caused by cirrhosis, a disease that results from scarring of the liver. Other causes of portal hypertension include blood clots in the portal vein, blockages of the veins that carry the blood from the liver to the heart, and a parasitic infection called schistosomiasis. Symptoms of portal hypertension include varices (enlarged veins), vomiting blood, blood in the stool, black and tarry stool, ascites (abnormal fluid collection within the peritoneum, the sac that contains the intestines within the abdominal cavity), confusion and lethargy, splenomegaly or enlargement of the spleen, and decreased white blood cell counts.
Hypertensive Kidney Disease
High blood pressure can damage the kidneys and is one of the leading causes of kidney failure (end-stage renal kidney disease). Kidney damage, like hypertension, can be unnoticeable and detected only through medical tests. If you have kidney disease, you should control your blood pressure. Other treatment options include prescription medications.
High Blood Pressure Treatment (Natural Home Remedies, Diet, Medications)
High blood pressure (hypertension) means high pressure (tension) in the arteries. Treatment for high blood pressure include lifestyle modifications (alcohol, smoking, coffee, salt, diet, exercise), drugs and medications such as ACE inhibitors, angiotensin receptor blockers, beta blockers, diuretics, calcium channel blockers (CCBs), alpha blockers, clonidine, minoxidil, and Exforge.
What Is High Blood Pressure (Hypertension)?
High blood pressure or hypertension is when the blood pressure readings consistently range from 140 or higher for systolic or 90 or higher for diastolic. Blood pressure readings above 180/120 mmHg are dangerously high and require immediate medical attention.
High Blood Pressure Symptoms
Most people with high blood pressure have no signs or symptoms, even if blood pressure readings reach dangerously high levels. In some patients, symptoms may include fatigue, headaches, dizziness, confusion, sweating, chest pain and vision problems.
Hypertension-Induced Chronic Kidney Disease
Hypertension-induced chronic kidney disease (CKD) is a long-standing kidney condition that develops over time due to persistent or uncontrolled high blood pressure (hypertension).
Treatment & Diagnosis
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