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Rituxan Rituximab MabThera PDF Print E-mail

Rituxan is a monoclonal antibody that is used for the treatment of certain types of non-Hodgkin's lymphoma.

As with any treatment, side effects are a risk with Rituxan (rituximab). The most common side effects that occur during Rituxan infusions include:
Rituximab Rituxan MabThera

Common Side Effects of Rituxan - Rituximab:

headache

fever

chills and shake

itching

hives

sneezing

throat irritation or tightness

nausea

cough

 

Other side effects may include:

aching joints

upper respiratory tract infection

decreased blood cell counts

lung problems

 

About Rituxan Dose:

  • As an infusion into a vein (intravenous, IV), over about 6 hours.  The time of the infusion may be shortened, depending on whether or not you have received Rituxan in the past, or how well you tolerate Rituxan.
  • Medications may be given just before the infusion to reduce the occurrence of infusion-related symptoms.
  • There is no pill form of Rituxan.
  • The amount of Rituxan you will receive depends on many other factors, including your height and weight, your general health or other health problems, and the type of cancer you have. Your doctor will determine your dosage and schedule.

Rituximab Rituxan MabThera

Rituxan Self Care Tips:

  • Rituxan may cause temporary low blood pressure.  If you are taking medication to reduce your blood pressure, check with your doctor or nurse as to whether you should take it as usual or not before the infusion.

  • You may experience shortness of breath, feel flushed or dizzy during the infusion. You will most likely receive medication before the infusion, and you will be closely monitored during the infusion. 
  • For flu-like symptoms, keep warm with blankets and drink plenty of liquids.  There are medications that can help reduce the discomfort caused by chills.

  • Drink 2 to 3 quarts of fluid for the first 48 hours after each infusion, unless you were told to restrict your fluid intake. 
  • Rituxan infrequently causes nausea. But if you should experience nausea, take anti-nausea medications as prescribed by your doctor, and eat small, frequent meals. Sucking on lozenges and chewing gum may also help.

  • You may experience drowsiness or dizziness; avoid driving or engaging in tasks that require alertness until your response to the drug is known.
  • In general, drinking alcoholic beverages should be avoided. 

 

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Aranesp Darbepoetin Alfa Dose and Affects PDF Print E-mail

Aranesp® (darbepoetin alfa) For Injection

What Aranesp Is Used For:  Aranesp is a support medication. It does not treat cancer.   Aranesp is used to treat anemia caused by chemotherapy cancer treatment. Aranesp is not indicated for patients with myeloid cancers (cancers that originate in the bone marrow such as leukemia).   Aranesp is not appropriate for the treatment of anemia from other causes such as iron or folate deficiency or gastrointestinal bleeding.  Aranesp is not a substitute for blood transfusion.Aranesp Darepoetin alfa

Informatin on Aranesp Side Effects:  Keep in mind that most people do not experience all of the Aranesp side effects listed.  Aranesp side effects are almost always reversible and will go away after treatment is complete. There is no relationship between the presence or severity of Aranesp side effects and the effectiveness of Aranesp. Aranesp side effects are often predictable in terms of their onset and duration.  There are many options to help minimize or prevent Aranesp side effects.  Aranesp side effects may also be attributed to the cancer and/or chemotherapy treatment.

Common Aranesp side effects:

  • Fatigue

Less Common Aranesp side effects:

  • Edema (swelling, usually in the feet or hands)
  • Fever
  • Dizziness
  • Headache
  • Diarrhea
  • Constipation
  • Nausea
  • Vomiting
  • Joint pain
  • Shortness of breath

Aranesp - darbepoetin alfa

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Risperdal Side Effects and Risperdal Effects PDF Print E-mail

Risperdal -  Generic Name: risperidone

Risperdal is an antipsychotic drug that was approved to treat symptoms of schizophrenia.  It may, as with all medicines, cause some side effects.Risperdal - Risperidone

Most common Risperdal side effects :  Anxiety; constipation; cough; diarrhea; dizziness; drowsiness; dry mouth; fatigue; headache; increased appetite; increased saliva production; lightheadedness; nausea; restlessness; runny nose; stomach pain or upset; trouble sleeping; vomiting; weight gain

Severe Risperdal side effects:  Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); abnormal thoughts; confusion; decreased sexual ability; drooling; enlarged breasts; fainting; fast or irregular heartbeat; fever; inability to control urination; increased sweating; missed menstrual period; new or worsening mental or mood changes (eg, aggression, agitation, severe anxiety); nipple discharge; prolonged painful erection; seizures; severe dizziness; stiff or rigid muscles; suicidal thoughts or attempts; symptoms of high blood sugar (eg, increased thirst, hunger, or urination; unusual weakness); tremor; trouble concentrating, speaking, or swallowing; trouble sitting still; trouble walking or standing; uncontrolled muscle movements (eg, arm or leg movements, twitching of the face or tongue, jerking or twisting); unusual bruising; vision changes.

 

Bipolar Mania In the US placebo-controlled trial with risperidone as monotherapy, approximately 8% (10/134) of Risperdal®-treated patients discontinued treatment due to an adverse event, compared with approximately 6% (7/125) of placebo-treated patients. The adverse events associated with discontinuation and considered to be possibly, probably, or very likely drug-related included paroniria, somnolence, dizziness, extrapyramidal disorder, and muscle contractions involuntary. Each of these events occurred in one Risperdal®-treated patient (0.7%) and in no placebo-treated patients (0%).

 

In the US placebo-controlled trial with risperidone as adjunctive therapy to mood stabilizers, there was no overall difference in the incidence of discontinuation due to adverse events (4% for Risperdal® vs. 4% for placebo).
 

Incidence in Controlled Trials

Commonly Observed Adverse Events in Controlled Clinical Trials

 

Schizophrenia

In two 6- to 8-week placebo-controlled trials, spontaneously-reported, treatment-emergent adverse events with an incidence of 5% or greater in at least one of the Risperdal® groups and at least twice that of placebo were anxiety, somnolence, extrapyramidal symptoms, dizziness, constipation, nausea, dyspepsia, rhinitis, rash, and tachycardia.

 

Adverse events were also elicited in one of these two trials (i.e., in the fixed-dose trial comparing Risperdal® at doses of 2, 6, 10, and 16 mg/day with placebo) utilizing a checklist for detecting adverse events, a method that is more sensitive than spontaneous reporting. By this method, the following additional common and drug-related adverse events occurred at an incidence of at least 5% and twice the rate of placebo: increased dream activity, increased duration of sleep, accommodation disturbances, reduced salivation, micturition disturbances, diarrhea, weight gain, menorrhagia, diminished sexual desire, erectile dysfunction, ejaculatory dysfunction, and orgastic dysfunction.

 

Bipolar Mania -  In the United States  placebo-controlled trial with risperidone as monotherapy, the most commonly observed adverse events associated with the use of Risperdal® (incidence of 5% or greater and at least twice that of placebo) were somnolence, dystonia, akathisia, dyspepsia, nausea, parkinsonism, vision abnormal, and saliva increased. In the US placebo-controlled trial with risperidone as adjunctive therapy to mood stabilizers, the most commonly observed adverse events associated with the use of Risperdal® were somnolence, dizziness, parkinsonism, saliva increased, akathisia, abdominal pain, and urinary incontinence.

 

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Enbrel Etanercept Treatment Embrel PDF Print E-mail

ENBREL (etanercept) For subcutaneous injection. 

ENBREL is for reducing signs and symptoms of moderately to severely active rheumatoid arthritis; severely active polyarticular juvenile idiopathic arthritis; inhibiting the progression of structural damage of active arthritis, and improving phEnbrelysical function in patients with psoriatic arthritis;  ENBREL® is indicated for reducing signs and symptoms in patients with active ankylosing spondylitis.  It is also  indicated for the treatment of adult patients with chronic moderate to severe plaque psoriasis who are candidates for systemic therapy or phototherapy.

 ENBREL can be initiated in combination with methotrexate (MTX) or used alone.

Side Effects of Enbrel all medicines may cause side effects, but many people have no, or minor side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome when using Enbrel Multiple-Use Vials:

Dizziness; headache; pain, redness, itching, bruising, or swelling around the injection site.

Seek medical attention right away if any of these SEVERE side effects occur when using Enbrel: Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); butterfly rash (rash on nose and cheeks); chest pain or discomfort; decreased mental alertness; fast heartbeat; fever, chills, or sore throat; general feeling of being unwell; mental or mood changes; new or worsening cough; numbness or tingling throughout your body; rapid breathing; rash on your face and arms that gets worse in the sun; seizures; shortness of breath; swelling of arms or legs; swelling of the lymph nodes; unusual bruising or bleeding; unusual lumps; unusual nausea, vomiting, stomach pain, or diarrhea; unusual tiredness; vision problems; weakness in arms or legs.

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Remicade Infliximab - Chrons Disease Arthritis PDF Print E-mail

Remicade - Infliximab

Infliximab Remicade

 

Most Common Remicade Infliximab Side Effects

Abdominal pain ; cough ; dizziness ; sneezing ; fainting ; headache ; muscle pain ; nasal congestion ; nausea ; runny nose ;

shortness of breath ; sore throat ; tightness in chest ; unusual tiredness or weakness ; vomiting ;wheezing

 

Less Common Remicade (Infliximab) Side Effects

Back pain ; bloody or cloudy urine ; cracks in skin at the corners of mouth ; diarrhea difficult or; painful urination ; frequent urge to urinate ; high blood pressure ; low blood pressure ; pain

pain or tenderness around eyes and cheekbones ; skin rash ;soreness or irritation of mouth or tongue ; soreness or redness around fingernails or toenails ; vaginal burning or itching and discharge ; white patches in mouth and/or on tongue

 

Remicade - Infliximab

Crohn's Disease Remicade or Fistulizing Crohn's Disease and Infliximab - The recommended dose of  Remicade is 5 mg/kg given as an intravenous induction regimen at 0, 2 and 6 weeks followed by a maintenance regimen of 5 mg/kg every 8 weeks thereafter for the treatment of adults with moderately to severely active Crohn's disease or fistulizing Crohn's disease. For adult patients who respond and then lose their response, consideration may be given to treatment with 10 mg/kg. Patients who do not respond by week 14 are unlikely to respond with continued dosing and consideration should be given to discontinue REMICADE in these patients.
 

Remicade Arthritis - Rheumatoid Remicade in combination with methotrexate, is indicated for reducing signs and symptoms, inhibiting the progression of structural damage, and improving physical function in patients with moderately to severely active rheumatoid arthritis.

 

Remicade Arthritis - Psoriatic :  Remicade is indicated for reducing the sings and symptoms of active arthritis by inhibiting the progression of structural damage and improving physicial function in patients with psoriatic arthritis.

Ulcerative Colitis - REmicade is indicated for reducing signs and symptoms, inducing and maintaining clinical remission and mucosal healing, and eliminating corticosteroid use in patients with moderately to severely active ulcerative colitis who have had an inadequate response to conventional therapy.

____________________________

Remicade injection  - lyophilized concentrate for IV injection is supplied in individually-boxed single-use vials in the following strength:

NDC 57894-030-01.......................100 mg infliximab in a 20 mL vial

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Medication Norvasc and NorvascTablet Problems PDF Print E-mail

Brand Name: Norvasc    Generic Name: amlodipine

Based on the studies, the most common Norvasc Side Effects are:Norvasc

  • Swelling or water retention (edema) -- in up to 10.8 percent of people
  • Feelings of a rapidly or forcefully beating heart (heart palpitations) -- up to 4.5 percent
  • Fatigue -- up to 4.5 percent
  • Dizziness -- up to 3.4 percent
  • Nausea -- up to 2.9 percent
  • Flushing (redness of the skin, especially the face) -- up to 2.6 percent
  • Abdominal pain (stomach pain) -- up to 1.6 percent
  • Drowsiness -- up to 1.4 percent.

Norvasc has been studied thoroughly in clinical trials in which a group of people taking the drug have side effects documented and compared to another group not taking the medicine.

Side Effects by Body System

General  -  Norvasc - Amlodipine is generally well-tolerated at dosages up to 10 mg per day. Most side effects reported were of mild or moderate severity and were dose-related. Headache and edema are the most common side effects.Norvasc

Other -  Other side effects have included edema (up to 14.6%), flushing (up to 4.5%), fatigue (4.5%), and back pain (up to 2%). Allergic reaction, asthenia, hot flushes, malaise, pain, rigors, tinnitus, weight decrease, and weight gain have been reported in less than 1% but greater than 0.1% of patients. Cold and clammy skin and parosmia have been reported in less than 0.1% of patients. A single case of acute porphyria exacerbation has been associated with the use of amlodipine, and confirmed upon rechallenge in the same patient. Calcium channel blockers have been suggested as possibly unsafe in patients with this condition.

Cardiovascular  -  Cardiovascular side effects have included palpitation (up to 4.5%) and peripheral edema (2%). Peripheral edema may become a chronic problem, and may occur in up to 10% of patients who are receiving 10 mg doses. Arrhythmia (including ventricular tachycardia and atrial fibrillation), bradycardia, chest pain, hypotension, peripheral ischemia, postural dizziness, postural hypotension, syncope, tachycardia, and vasculitis have been reported in less than 1% but greater than 0.1% of patients. Cardiac failure, extrasystoles, and pulse irregularity have been reported in less than 0.1% of patients. Angina and myocardial infarction have occasionally been reported; however, these reactions could not be distinguished from coexisting disease states or medications. Worsened angina has been rarely associated with the use of amlodipine (as with other calcium channel blockers).

Recent data have shown that the use of amlodipine in patients with NYHA Class III or IV heart failure is not associated with worsened heart failure.

Nervous system

Nervous system side effects have included headache (7.3%), dizziness (up to 3.4%), and somnolence (1.6%). Hypoesthesia, paresthesia, peripheral neuropathy, tremor, and vertigo have been reported in less than 1% but greater than 0.1% of patients. Ataxia and migraine have been reported in less than 0.1% of patients. Myoclonus has been reported.

Gastrointestinal

Gastrointestinal side effects have included nausea (2.9%), dysphagia (up to 2%), and abdominal pain (1.6%). Anorexia, constipation, diarrhea, dry mouth, dyspepsia, flatulence, gingival hyperplasia, pancreatitis, and vomiting have been reported in less than 1% but greater than 0.1% of patients. Gastritis, increased appetite, loose stools, and taste perversion have been reported in less than 0.1% of patients. At least one case of amlodipine-associated dysgeusia has been reported and confirmed upon rechallenge.

Hematologic

A case study reports a 34-year-old woman with a history of chronic renal failure secondary to glomerulonephritis, who was started on amlodipine for uncontrolled hypertension. Three days later the patient developed severe thrombocytopenia. After discontinuation of the drug, the platelet count returned to normal.

Hematologic side effects have included leukopenia, purpura, and thrombocytopenia in less than 1% but greater than 0.1% of patients.

Hepatic

Hepatic side effects have included jaundice and hepatic enzyme elevations (mostly consistent with cholestasis or hepatitis) during postmarketing experience. In some instances, these cases were severe enough to require hospitalization.

Dermatologic

Dermatologic side effects have included rash and erythematous rash in up to 2% of patients and angioedema, erythema multiforme, increased sweating, maculopapular rash, and pruritus in less than 1% but greater than 0.1% of patients. Alopecia, dermatitis, skin discoloration, skin dryness, and urticaria have been reported in less than 0.1% of patients. Amlodipine-associated lichen planus and telangiectasia have been rarely reported.

Genitourinary

Genitourinary side effects have included micturition disorder, micturition frequency, and nocturia in less than 1% but greater than 0.1% of patients. Dysuria and polyuria have been reported in less than 0.1% of patients.

Hypersensitivity

Hypersensitivity side effects have included at least one case of erythema multiforme. Hypersensitivity reactions have rarely been reported, although experience with amlodipine is limited.

A 62-year-old man with hypertension and psoriasis developed erythema multiforme within three days after starting amlodipine. The rash resolved upon substitution with nifedipine.

Endocrine

In one case, a patient's gynecomastia resolved upon substitution of amlodipine with an unrelated antihypertensive agent.

Endocrine side effects have included gynecomastia during postmarketing experience.

Renal

Renal side effects have been reported rarely. At least one case of interstitial nephritis has been associated with amlodipine therapy.

 This way, it is possible to see what side effects occur, how often they appear, and how they compare to the group not taking the medicine.

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Nexium Esomeprazole Magnesium Side Effects PDF Print E-mail

Brand Name: NexiumNexium - Esomeprazole

Generic Name: esomeprazole (ee so MEP ra zol)

 

Nexium decreases the amount of acid produced in the stomach. Nexium is used to treat symptoms of gastroesophageal reflux disease (GERD) and other conditions involving excessive stomach acid such as Zollinger-Ellison syndrome. It is also used to promote healing of erosive esophagitis (damage to your esophagus caused by stomach acid).  

 

Nexium may also be given to prevent gastric ulcer caused by infection with helicobacter pylori (H. pylori), or by the use of nonsteroidal anti-inflammatory drugs (NSAIDs).  Nexium may also be used for purposes other than those listed in it's medication guide.

Nexium Side Effects

Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat.  Other less serious Nexium side effects are more likely to occur, such as:

  • headache;

  • diarrhea;

  • nausea, stomach pain, gas, constipation; or

  • dry mouth.

Side effects other than those listed here may also occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

What other drugs will affect Nexium?

Before taking Nexium, tell your doctor if you are using any of the following drugs:

  • clopidogrel (Plavix);

  • digoxin (Lanoxin, Lanoxicaps);

  • diazepam (Valium);

  • ketoconazole (Nizoral);

  • HIV or AIDS medication such as atazanavir (Reyataz), nelfinavir (Viracept), saquinavir (Invirase), and others;

  • iron (Feosol, Mol-Iron, Fergon, Femiron, others); or

  • a blood thinner such as warfarin (Coumadin).

If you are using any of these drugs, you may not be able to use Nexium, or you may need dosage adjustments or special tests during treatment.

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