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Mega-Trim Side Effects

Generic name: phenylpropanolamine

Note: This document contains side effect information about phenylpropanolamine. Some dosage forms listed on this page may not apply to the brand name Mega-Trim.

Applies to phenylpropanolamine: oral capsule extended release, oral tablet, oral tablet extended release.

Warning

Phenylpropanolamine has been associated with an increased risk of hemorrhagic stroke (bleeding into the brain or into tissue surrounding the brain) in women. Men may also be at risk. Although the risk of hemorrhagic stroke is low, the U.S. Food and Drug Administration (FDA) recommends that consumers not use any products that contain phenylpropanolamine.

Do not take phenylpropanolamine for longer than 7 days if your condition does not improve or if your symptoms are accompanied by a high fever.

Do not take more of this medication than is recommended on the package or by your doctor.

Use caution when driving, operating machinery, or performing other hazardous activities. Phenylpropanolamine may cause dizziness or drowsiness. If you experience dizziness or drowsiness, avoid these activities.

If you experience any of the following serious side effects from this medication, stop taking phenylpropanolamine (the active ingredient contained in Mega-Trim) and seek emergency medical attention:

Other, less serious side effects may be more likely to occur. Continue to take phenylpropanolamine and talk to your doctor if you experience

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.

For Healthcare Professionals

Applies to phenylpropanolamine: oral capsule extended release, oral tablet, oral tablet extended release.

Cardiovascular

Cardiovascular adverse effects may be associated with phenylpropanolamine (the active ingredient contained in Mega-Trim) Phenylpropanolamine can cause a significant rise in heart rate. Hypertension and arrhythmias may be problematic in susceptible patients. Cardiovascular side effects have also included an increased risk of hemorrhagic stroke.[Ref]

Phenylpropanolamine causes vasoconstriction which usually does not result in blood pressure elevations in healthy adults given normally prescribed dosages. However, phenylpropanolamine administration may be problematic for patients with preexisting hypertension and those receiving higher dosages. In general, 75-mg of sustained-release phenylpropanolamine will not produce a significant increase in blood pressure in normotensive patients, but 150-mg of sustained-release phenylpropanolamine can.

The combination of caffeine and phenylpropanolamine is more apt to cause hypertension. Although caffeine is no longer added to phenylpropanolamine as an anorexiant, this combination is available as "look-alikes" for amphetamines. Hypertensive crisis has occurred occasionally subsequent to overuse, overdose, and ingestion of normally recommended doses. Hypertensive crisis may be accompanied by headache, blurred vision, confusion, intracranial hemorrhage, encephalopathy, or seizures.

Arrhythmias may be produced in predisposed patients. The majority of reports of arrhythmias involve overuse or overdose. Rarely, high doses of phenylpropanolamine may cause chest pain and evidence of myocardial injury.

One study reported that taking phenylpropanolamine increases the risk of hemorrhagic stroke in women. Men may also be at risk. Although the risk of hemorrhagic stoke is very low, the FDA recommends that all use of phenylpropanolamine be discontinued.[Ref]

Nervous system

Seizures may occur in rare cases of hypertensive crisis and have been reported with normally recommended doses as well as in cases of overuse or overdose.

There have been anecdotal reports of cerebrovascular hemorrhage largely associated with an uneven pattern of cerebrovascular spasm referred to as vascular beading. Vascular beading has also been reported in the absence of hemorrhage. Intracranial hemorrhage has almost always been associated with hypertension.[Ref]

Phenylpropanolamine produces nervous system stimulation, resulting in tremor, anxiety, insomnia, dizziness, and nervousness. Headache may also occur.[Ref]

Psychiatric

Psychiatric reactions occur infrequently but include acute mania, anxiety, paranoia, confusion, agitation, and hallucinations. These reactions may be more common in women.[Ref]

Psychotic reactions to phenylpropanolamine have occurred in patients receiving normally recommended doses and in cases of abuse. In a few patients, phenylpropanolamine appears to have exacerbated an underlying bipolar disorder which was previously undiagnosed.

A psychotic episode consisting of abnormal behavior was reported in a young woman following a week of therapy with Naldecon (phenylephrine, phenylpropanolamine, chlorpheniramine, and phenyltoloxamine) and amantadine. The patient had no personal or family history of psychiatric illness and no history of recreational substance use. It is uncertain whether the episode was due to the amantadine, the phenylpropanolamine, or another component in the Naldecon, or if it was an interaction between the drugs.[Ref]

Gastrointestinal

Gastrointestinal adverse effects most commonly seen are anorexia and gastric irritation. Nausea and vomiting have occurred in conjunction with hypertensive episodes.[Ref]

Hypersensitivity

Hypersensitivity reactions to phenylpropanolamine (the active ingredient contained in Mega-Trim) may occur.[Ref]

Renal

Rarely, phenylpropanolamine (the active ingredient contained in Mega-Trim) may cause acute interstitial nephritis.[Ref]

References

1. Lake CR, Gallant S, Masson E, Miller P. Adverse drug effects attributed to phenylpropanolamine: a review of 142 case reports. Am J Med. 1990;89:195-208.

2. Lake CR, Zaloga G, Bray J, Rosenberg D, Chernow B. Transient hypertension after two phenylpropanolamine diet aids and the effects of caffeine: a placebo-controlled follow-up study. Am J Med. 1989;86:427-32.

3. Lake CR, Zaloga G, Clymer R, Quirk RM, Chernow B. A double dose of phenylpropanolamine causes transient hypertension. Am J Med. 1988;85:339-43.

4. Bernstein E, Diskant BM. Phenylpropanolamine: a potentially hazardous drug. Ann Emerg Med. 1982;11:311-5.

5. Kroenke K, Omori DM, Simmons JO, Wood DR, Meier NJ. The safety of phenylpropanolamine in patients with stable hypertension. Ann Intern Med. 1989;111:1043-4.

6. Pentel PR, Mikell FL, Zavoral JH. Myocardial injury after phenylpropanolamine ingestion. Br Heart J. 1982;47:51-4.

7. Howrie DL, Wolfson JH. Phenylpropanolamine-induced hypertensive seizures. J Pediatr. 1983;102:143-5.

8. Horowitz JD, Lang WJ, Howes LG, Fennessy MR, Christophidis N, Rand MJ, Louis WJ. Hypertensive responses induced by phenylpropanolamine in anorectic and decongestant preparations. Lancet. 1980;1:60-1.

9. McEwen J. Phenylpropanolamine-associated hypertension after the use of "over- the-counter" appetite-suppressant products. Med J Aust. 1983;2:71-3.

10. Mueller SM. Neurologic complications of phenylpropanolamine use. Neurology. 1983;33:650-2.

11. Clark JE, Simon WA. Cardiac arrhythmias after phenylpropanolamine ingestion. Drug Intell Clin Pharm. 1983;17:737-8.

12. Noble R. A controlled clinical trial of the cardiovascular and psychological effects of phenylpropanolamine and caffeine. Drug Intell Clin Pharm. 1988;22:296-9.

13. O'Connell MB, Gross CR. The effect of multiple doses of phenylpropanolamine on the blood pressure of patients whose hypertension was controlled with beta blockers. Pharmacotherapy. 1991;11:376-81.

14. O'Connell MB, Gross CR. The effect of single-dose phenylpropanolamine on blood pressure in patients with hypertension controlled by beta blockers. Pharmacotherapy. 1990;10:85-91.

15. Chin C, Choy M. Cardiomyopathy induced by phenylpropanolamine. J Pediatr. 1993;123:825-7.

16. Leo PJ, Hollander JE, Shih RD, Marcus SM. Phenylpropanolamine and associated myocardial injury. Ann Emerg Med. 1996;28:359-62.

17. Kizer KW. Intracranial hemorrhage associated with overdose of decongestant containing phenylpropanolamine Am J Emerg Med. 1984;2:180-1.

18. Edwards M, Russo L, Harwood-Nuss A. Cerebral infarction with a single oral dose of phenylpropanolamine. Am J Emerg Med. 1987;5:163-4.

19. Cornelius JR, Soloff PH, Reynolds CF, 3d. Paranoia, homicidal behavior, and seizures associated with phenylpropanolamine. Am J Psychiatry. 1984;141:120-1.

20. Achor MB, Extein I. Diet aids, mania, and affective illness Am J Psychiatry. 1981;138:392.

21. Schaffer CB, Pauli MW. Psychotic reaction caused by proprietary oral diet agents. Am J Psychiatry. 1980;137:1256-7.

22. Grieger TA, Clayton AH, Goyer PF. Affective disorder following use of phenylpropanolamine Am J Psychiatry. 1990;147:367-8.

23. Dietz AJ, Jr. Amphetamine-like reactions to phenylpropanolamine. JAMA. 1981;245:601-2.

24. Norvenius G, Widerlov E, Lonnerholm G. Phenylpropanolamine and mental disturbances Lancet. 1979;2:1367-8.

25. Johnson DA, Etter HS, Reeves DM. Stroke and phenylpropanolamine use Lancet. 1983;2:970.

26. Elliott CF, Whyte JC. Phenylpropanolamine and hypertension. Med J Aust. 1981;1:715.

27. Maher LM, Peterson PL, Dela-Cruz C. Postpartum intracranial hemorrhage and phenylpropanolamine use Neurology. 1987;37:1686.

28. Kase CS, Foster TE, Reed JE, Spatz EL, Girgis GN. Intracerebral hemorrhage and phenylpropanolamine use. Neurology. 1987;37:399-404.

29. Kikta DG, Devereaux MW, Chandar K. Intracranial hemorrhages due to phenylpropanolamine. Stroke. 1985;16:510-2.

30. Lake CR, Tenglin R, Chernow B, Holloway HC. Psychomotor stimulant-induced mania in a genetically predisposed patient: a review of the literature and report of a case. J Clin Psychopharmacol. 1983;3:97-100.

31. Stroe AE, Hall J, Amin F. Psychotic episode related to phenylpropanolamine and amantadine in a healthy female. Gen Hosp Psychiatry. 1995;17:457-8.

32. Marshall RD, Douglas CJ. Phenylpropanolamine-induced psychosis: potential predisposing factors. Gen Hosp Psychiatry. 1994;16:358-60.

33. Speer F, Carrasco LC, Kimura CC. Allergy to phenylpropanolamine. Ann Allergy. 1978;40:32-4.

34. Singer DR, Simpson JG, Catto GR, Johnston AW. Drug hypersensitivity causing granulomatous interstitial nephritis. Am J Kidney Dis. 1988;11:357-9.

35. Swenson RD, Golper TA, Bennett WM. Acute renal failure and rhabdomyolysis after ingestion of phenylpropanolamine-containing diet pills. JAMA. 1982;248:1216.

36. Neveus T, Tuvemo T, Lackgren G, Stenberg A. Bladder capacity and renal concentrating ability in enuresis: Pathogenic implications. J Urol. 2001;165:2022-5.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Some side effects may not be reported. You may report them to the FDA.