Azithromycin (Zithromax Z-pack) is a pre-packaged form of a macrolide antibacterial Azithromycin (brand
name; Zithromax or Zmax). Zithromax should only be used in mild to
moderate infections that are strongly suspected or proven when culture
information is available to be caused by susceptible bacteria, e.g.,
Chlamydia trachomatis.
Macrolide antibiotic drug is a class of antibiotics that include Erythromycin, Biaxin, Clarithromycin, Ery-Tab.
Indications for Zithromax:
Active ingredient is Azithromycin Dihydrate 600 mg in 1 tablet
Inactive ingredients:
Active ingredient is 1 gm Azithromycin Dihydrate in a single-dose package of 5ml
Inactive ingredients:
In March 2013, FDA issued a warning concerning a potential risk of Azithromycin (Zithromax or Zmax). Azithromycin can cause abnormal changes in the electrical activity of the heart that may lead to a potentially fatal irregular heart rhythm. Patients who are at high risk of developing this condition include those with the conditions stated below:
The result of this study showed an increase in cardiovascular deaths and in the risk of death in patients treated with a 5-day course of Azithromycin (Zithromax) and Levofloxacin compared to persons treated with Amoxicillin, Ciprofloxacin, or no drug.
Side effects reported in adults and pediatric patients include:
Before taking this pharmaceutical, consider the potential benefits and risks to other alternative options.
Macrolide antibiotic drug is a class of antibiotics that include Erythromycin, Biaxin, Clarithromycin, Ery-Tab.
Indications for Zithromax:
- Non-gonococcal cervicitis and urethritis due to Chlamydia trachomatis
- Prophylaxis of disseminated avian complex (MAC) disease
in person with advanced HIV infection
Active ingredient is Azithromycin Dihydrate 600 mg in 1 tablet
Inactive ingredients:
- Sodium croscarmellose
- Magnesium stearate
- Dibasic calcium phosphate anhydrous
- An aqueous film coat consisting of hypromellose
- Titanium dioxide
- Lactose
- Triacetin
- Pregelatinized starch
- Sodium lauryl sulfate
Active ingredient is 1 gm Azithromycin Dihydrate in a single-dose package of 5ml
Inactive ingredients:
- Colloidal silicon dioxide
- Sodium phosphate tribasic
- Dried artificial banana flavor
- Dried artificial cherry flavor
- Sucrose
In March 2013, FDA issued a warning concerning a potential risk of Azithromycin (Zithromax or Zmax). Azithromycin can cause abnormal changes in the electrical activity of the heart that may lead to a potentially fatal irregular heart rhythm. Patients who are at high risk of developing this condition include those with the conditions stated below:
- QT interval prolongation
- Low blood levels of magnesium
- Low blood levels of potassium
- Slow heart rate
- Using certain drugs to treat abnormal heart rhythms
- Arrhythmias
The result of this study showed an increase in cardiovascular deaths and in the risk of death in patients treated with a 5-day course of Azithromycin (Zithromax) and Levofloxacin compared to persons treated with Amoxicillin, Ciprofloxacin, or no drug.
Side effects reported in adults and pediatric patients include:
- Angioedema (deep skin layer hives-liked)
- Arthralgia (joint pain)
- Cholestatic jaundice
- Nausea, vomiting, diarrhea
- Abdominal pain
- Chest pain
- Palpitation (irregular/forceful beating of the heart)
- Dyspepsia (indigestion)
- Flatulence (excessive gas in the intestinal tract)
- Melena (stool or vomit that is black due to blood pigment)
- Vaginitis
- Nephritis (inflammation of the kidney)
- Dizziness, headache, vertigo, convulsion
- Semnolence (sleepiness)
- Rash
- Photosensitivity
- Arthralgia (joint pain)
- Urticaria (hives)
- Arrhythmias
- Tachycardia (rapid heart rate greater than 100 beats)
- Hypotension
- Anorexia (an eating disorder, markedly reduce appetite
- Constipation
- Pseudomembranous colitis (severe inflammation of the inner lining of the colon)
- Pancreatitis
- Oral candidiasis
- Pyloric stenosis (narrowing passage between the stomach and duodenum)
- Tongue discoloration
- Asthenia (weakness, lack of energy and strength)
- Paresthesia (numbness, tingling, burning sensation)
- Anaphylaxis (allergic reaction)
- Thrombocytopenia (low platelets count)
- Hepatic necrosis (death of liver cells or tissues)
- Hepatic failure
- Nervousness, agitation
- Syncope (partial or complete loss of consciousness)
- Anxiety and aggressive reaction
- Pruritus (itching)
- Erythema multiforme
- Stevens-Johnson syndrome
- Toxic epidermal necrolysis
- Hearing loss, deafness, tinnitus
Before taking this pharmaceutical, consider the potential benefits and risks to other alternative options.
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