Drug Uses
Zithromax is used to treat many different types of bacterial infections, such as bronchitis, pneumonia, tonsillitis, skin infections, ear infections, and sexually transmitted diseases.
How Taken
Zithromax comes as a capsule, tablet, and liquid to take it orally. It is usually taken once a day for 2-5 days. Take Zithromax exactly as directed. Do not take more or less of it or take it more often than prescribed by your doctor. Shake the liquid well before each use to mix the medication evenly. The capsules and tablets should be taken with a full glass of water. Continue to take Zithromax even if you feel well. Do not stop taking Zithromax without talking to your doctor. Take Zithromax liquid at least 1 hour before or 2 hours after meals. The capsule and tablet may be taken with or without food. If it upsets your stomach, take it with food.
Warnings/Precautions
Before taking Zithromax, tell your doctor if you have liver disease. You may not be able to take Zithromax, or you may require a lower dose or special monitoring during treatment.
Zithromax is in the FDA pregnancy category B. This means that it is not expected to harm an unborn baby. Do not take this medication without first talking to your doctor if you are pregnant or could become pregnant during treatment.
It is not known whether Zithromax passes into breast milk. Do not take this medication without first talking to your doctor if you are breast-feeding a baby
Missed Dose
Take the missed dose as soon as you remember. However, if it is almost time for the next regularly scheduled dose, skip the missed dose and take the next one as directed. Do not take a double dose of this medication unless otherwise directed by your doctor.
Possible Side Effects
If you experience any of the following serious side effects, stop taking Zithromax and seek emergency medical attention: an allergic reaction (difficulty breathing; closing of the throat; swelling of the lips, tongue, or face; or hives); or liver damage (yellowing of the skin or eyes, nausea, abdominal pain or discomfort, unusual bleeding or bruising, severe fatigue).
Other, less serious side effects may be more likely to occur. Continue to take Zithromax and talk to your doctor if you experience nausea, vomiting, diarrhea, or abdominal pain; unusual dizziness, fatigue, or headache; vaginal yeast infection; a rash; or increased sensitivity to sunlight.
Side effects other than those listed here may also occur. Talk to your doctor about any side effect that seems unusual or that is especially bothersome.
Storage
Zithromax tablets should be stored between 15° to 30° C (59° to 86°F).
Store constituted suspension between 5° to 30°C (41° to 86°F) and discard when full dosing is completed or within 10 days. Shake well before each use. Oversized bottle provides shake space. Keep tightly closed.
Overdose
Seek emergency medical attention. Symptoms of Zithromax overdose include nausea, vomiting, diarrhea, and abdominal discomfort.
More Information
Avoid prolonged exposure to sunlight. Zithromax may increase the sensitivity of the skin to sunlight. Use a sunscreen and wear protective clothing when exposure to the sun is unavoidable.
Disclaimer
This drug information is for your information purposes only, it is not intended that this information covers all uses, directions, drug interactions, precautions, or adverse effects of your medication. This is only general information, and should not be relied on for any purpose. It should not be construed as containing specific instructions for any particular patient. We disclaim all responsibility for the accuracy and reliability of this information, and/or any consequences arising from the use of this information, including damage or adverse consequences to persons or property, however such damages or consequences arise. No warranty, either expressed or implied, is made in regards to this information.
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(NaturalNews) The FDA has issued a call for "black box" warnings to be placed on certain antibiotics about the risk that they may cause tendonitis and ruptured tendons.
The antibiotics affected are those in the fluoroquinolone family, including Bayer's Cipro (generic name ciprofloxacin) and Avelox, Johnson & Johnson's Floxin (generic name ofloxacin) and Levaquin, Depomed's Proquin XR, Merck's Noroxin and Oscient's Factive.
These drugs already carry warning labels about tendons risks, but Edward Cox, FDA director of the microbial products office, said that "the FDA continues to receive a considerable number of reports of tendon-related adverse events. The FDA believes that these new labeling changes will better inform health-care providers and patients about the risk."
The black box warning is the strongest warning that the FDA can place on a drug before recalling it from the market.
The nonprofit consumer advocacy group Public Citizen saw the FDA in 2006 to demand a black box warning, and additionally directly notified doctors about the risk of tendon damage. The group had been urging the agency to issue such a warning since 1996.
Public Citizen cited government data showing 262 reports of ruptured tendons, 258 reports of tendonitis and 274 reports of other dependent problems as of late 2005 in those who had taken the drugs. A further 100 problems have reported since then, the group said.
The FDA concluded that the risk of tendon ruptures is three to four times higher in those who take the antibiotics than those they do not. Most at risk are patients over the age of 60, people using steroid therapy and those who have undergone certain organ transplants.
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