Lortab (Hydrocodone Bitartrate And Acetaminophen)
$280.00 – $1,650.00
WHAT IS Lortab (hydrocodone bitartrate and acetaminophen)?
Lortab (hydrocodone bitartrate and acetaminophen) is a prescription drug that is a controlled substance. It is classified as an opioid analgesic that is used to treat coughs and as a pain reliever. The primary ingredient in Lortab, which is also the opioid component, is hydrocodone.
Lortab also contains acetaminophen, and it’s available as a tablet, a liquid solution, and a syrup. An opioid is also often called a narcotic, and this particular narcotic, as with other opioids, can slow the respiratory system to the point where you stop breathing, or your breathing is slowed to a dangerous point.
this medicament is prescribed to patients for the treatment of moderate to severe pain.
Indications & Dosage
Lortab 10 (hydrocodone bitartrate and acetaminophen tablets) /500 tablets (Hydrocodone Bitartrate and Acetaminophen Tablets, USP, 10 mg/500 mg) are indicated for the relief of moderate to moderately severe pain.
DOSAGE AND ADMINISTRATION
Dosage should be adjusted according to severity of pain and response of the patient. However, it should be kept in mind that tolerance to hydrocodone can develop with continued use and that the incidence of untoward effects is dose related.
The usual adult dosage is one tablet every four to six hours as needed for pain. The total daily dosage should not exceed 6 tablets.
SIDE EFFECTS Lortab (Hydrocodone Bitartrate And Acetaminophen)
The most frequently reported adverse reactions are light-headedness, dizziness, sedation, nausea and vomiting. These effects seem to be more prominent in ambulatory than in non-ambulatory patients, and some of these adverse reactions may be alleviated if the patient lies down.
Other adverse reactions include:
Gastrointestinal System: Prolonged administration of Lortab 10 (hydrocodone bitartrate and acetaminophen tablets) /500 tablets may produce constipation.
Special Senses: Cases of hearing impairment or permanent loss have been reported predominantly in patients with chronic overdose.
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