28:08.08 Opiate Agonists
Drug Comments
ACETAMINOPHEN /  CODEINE  ELIXIR  
ACETAMINOPHEN /  CODEINE SUSPENSION  
ACETAMINOPHEN WITH CODEINE TABLET  
ALFENTANIL INJECTION
CODEINE  INJECTION
CODEINE TABLET  
FENTANYL 72 HOUR TRANSDERMAL PATCH

Transdermal fentanyl patches are contraindicated under the following conditions as serious life-threatening hypoventilation may occur: Management of acute or post-operative pain, including use in out patient surgeries. Management of mild or intermittent pain responsive to PRN or non-opioid therapy. Doses exceeding 25 mcg/h at the initiation of therapy in opioid-naïve patients. Children under 12 years of age or patients under 18 years of age who weigh less than 50 kg.

FENTANYL INJECTION Fentanyl PCA
HYDROCODONE /  ACETAMINOPHEN ELIXIR  
HYDROCODONE / ACETAMINOPHEN TABLET  
HYDROMORPHONE INJECTION  
HYDROMORPHONE TABLET  
LEVORPHANOL  INJECTION  
MEPERIDINE INJECTION PCA with meperidine doses greater than 10 mg/kg/day is not recommended or therapy for longer than 72 hours in patients with normal renal function.  Meperidine is not recommended in patients with renal dysfunction (creatinine clearance < 50 ml/min) or > 65 years old. Oral meperidine has high first pass metabolism, requiring a dose 3 times higher than injectable for equivalent analgesia. Conversion to normeperidine is increased when meperidine is administered by the oral route. Oral meperidine has high first pass metabolism, requiring a dose 3 times higher than injectable for equivalent analgesia. Conversion to normeperidine is increased when meperidine is administered by the oral route.
MEPERIDINE INJECTION,  PCA  300MG/30ML
MEPERIDINE SYRUP
MEPERIDINE TABLET
METHADONE TABLET  
MORPHINE INJECTION  
MORPHINE  INJECTION, EPIDURAL  
MORPHINE INJECTION,  PCA 30MG/30ML  
MORPHINE SOLUTION  
MORPHINE SOLUTION, CONCENTRATE  
MORPHINE TABLET  
MORPHINE TABLET,  SR  
OPIUM / BELLADONNA SUPPOSITORY  
OXYCODONE TABLET  
OXYCODONE SA TABLET  
OXYCODONE / ACETAMINOPHEN TABLET  
PROPOXYPHENE CAPSULE Propoxyphene and combination products containing propoxyphene are not recommended for use in pain management due to limited potency and accumulation of toxic metabolites (norpropoxyphene T1/2 39 hours, seizures, cardiac toxicity). Propoxyphene and norpropoxyphene have potent local anesthetic properties. Propoxyphene has a low therapeutic index and deaths have been reported with its use. Propoxyphene appears to display non-linear kinetics; steady state serum levels are 5-7 higher than those obtained after the first dose. Propoxyphene and norpropoxyphene are not removed by dialysis and naloxone is ineffective in treating cardiac toxicity. Alkalinization of the urine decreases propoxyphene excretion by 95%.
PROPOXYPHENE / ACETAMINOPHEN TABLET
SUFENTANIL INJECTION  
TRAMADOL TABLET  
   
   
   
   
   
   

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