What are the long term effects of Bactrim/Septra.?

Question

My mother (she's 50) has been on Bactrim for several years now due to reoccurent UTI caused by a bladder ulcer. What are the major concerns for taking this over the long term (other than bacteria resistant infections) Also she had an episode of tachycardia (160-172) for an hour and the next day she checked her B/P and it was 86/72. Her pulse is usually in the 60's and her B/P is normally 110/70-ish. Could this have anything to do with her long term Bactrim use? (And yes I already told her to go to the Dr.'s, she is there at this moment...I am just trying to find out for my own information) Thank you everyone who answers.

Answer 1

Sulfamethoxazole (as in Bactrim, Septra, Septrin etc)

Adverse effects and treatment

Nausea, vomiting, anorexia, and diarrhoea are relatively common following the administration of sulfamethoxazole and other sulfonamides.

Hypersensitivity reactions to sulfonamides have proved a problem. Fever is relatively common, and reactions involving the skin may include rashes, pruritis, photosensitivity reactions, exfoliative dermatitis, and erythema nodosum. Severe, potentially fatal, skin reactions including toxic epidermal necrolysis and the Stevens-Johnson syndrome have occurred in patients treated with sulfonamides. Dermatitis may also occur from contact of sulfonamides with the skin. Systemic lupus erythematosus, particularly exacerbation of pre-existing disease, has also been reported.

Nephrotoxic reactions including interstitial nephritis and tubular necrosis, which may result in renal failure, have been attributed to hypersensitivity to sulfamethoxazole. Lumbar pain, haematuria, oliguria, and anuria may also occur due to crystallisation in the urine of sulfamethoxazole or its less soluble acetylated metabolite. The risk of crystalluria can be reduced by the administration of fluids to maintain a high urine output. If necessary, alkalinisation of the urine by administration of sodium bicarbonate may increase solubility and aid the elimination of sulfonamides.

Blood disorders have occasionally occurred during treatment with the sulfonamides including sulfamethoxazole, and include agranulocytosis, aplastic anaemia, thrombocytopenia, leucopenia, hypothrombinaemia, and eosinophilia. Many of these effects on the blood may result from hypersensitivity reactions. Sulfonamides may rarely cause cyanosis due to methaemoglobinaemia. Acute haemolytic anaemia is a rare complication which may be associated with glucose-6-phosphate dehydrogenase deficiency.

Other adverse effects which may be manifestations of a generalised hypersensitivity reaction to sulfonamides include a syndrome resembling serum sickness, liver necrosis, hepatomegaly and jaundice, myocarditis, pulmonary eosinophilia and fibrosing alveolitis, and vasculitis including polyarteritis nodosa. Anaphylaxis has been reported only very rarely.

Other adverse reactions that have been reported after the administration of sulfamethoxazole or other sulfonamides include hypoglycaemia, hypothyrodism, neurological reactions including aseptic meningitis, ataxia, benign intracranial hypertension, convulsions, dizziness. drowsiness, fatigue, headache, insomnia, mental depression, peripheral or optic neuropathies, psychoses, tinnitus, vertigo, and pancreatitis.

Sulfonamides may displace serum-bound biluribin, resulting in jaundice and kernicterus in premature neonates.

As with other antimicrobials, sulfamethoxazole may cause alterations of the bacterial flora in the gastrointestinal tract. There is, therefore, the possibility, although it appears to be small, that pseudomembranous colitis may occur.

Slow acetylators of sulfamethoxazole may be at greater risk of adverse reactions than fast acetylators.

Precautions

In patients receiving sulfamethoxazole, adequate fluid intake is necessary to reduce the risk of crystalluria; the daily urine output should be 1200 to 1500 mL or more. The administration of compounds which render the urine acidic may increase the risk of crystalluria; the risk may be reduced with alkaline urine.

Treatment with sulfonamides should be discontinued immediately a rash appears because of the danger of severe allergic reactions such as the Stevens-Johnson syndrome.

Sulfamethoxazole should be given with care to patients with renal or hepatic impairment and is contra-indicated in patients with severe renal or hepatic failure or with blood disorders. Dosage reduction may be necessary in renal impairment. Complete blood counts and urinalyses with microscopic examination should be carried out particularly during prolonged therapy. Sulfamethoxazole should not be given to patients with a history of hypersensitivity to sulfonamides as cross-sensitivity may occur between drugs of this group. Care is generally advisable in patients with a history of allergy or asthma. Caution is also needed in the elderly, who may be more likely to have other risk factors for reactions. Some authorities consider sulfamethoxazole to be contra-indicated in lupus erythematosus as it may exacerbate the condition. Patients with glucose 6-phosphate dehydrogenase deficiency may be at risk of haemolytic reactions.

Sulfamethoxazole and other sulfonamides are not usually given to infants within 1 to 2 months of birth because of the risk of kernicterus; for the same reason, they are generally contra-indicated in women prior to delivery, and in breast-feeding mothers.

Patients with Aids may be particularly prone to adverse reactions, especially when sulfamethoxazole is given in combination with trimethoprim as co-trimoxazole.

Sulfonamides have been reported to interfere with some diagnostic tests, including those for urea, creatinine, and urinary glucose and urobilinogen.

Answer 2

I assume you know all the typical side effects such as hair loss (though not all chemo regimes cause hair loss), tiredness, nausea, depression etc- side effects vary from person to person. A few people breeze through it, others find it very difficult. It is three and a half years since I finished chemotherapy, and yes there can be some long term effects. I suffered a certain amount of mental confusion - what is often referred to as 'chemo brain' ; it affected my short term memory, including my memory for everyday words. Many chemo patients have amusing stories to tell about this; a few weeks after chemo ended I stood in a coffee shop struggling to remember the word for the sort of coffee I wanted - in the end I asked for 'unleaded'. The word decaff just wouldn't come. This can continue for some time after chemo ends; I still have attacks of 'chemo brain' but they are getting much fewer and far between. I had to leave a new job a year after chemo because I couldn't manage mental arithmetic and would get tearful trying. I don't have a problem with mental arithmetic now and I assume in time the occasional mental fogginess will end completely. Even if chemo brain never went away, I don't regret having chemotherapy. I'm fit and well and as far as I know cancer-free.

Answer 3

Septra Side Effects

Answer 4

Wow! That's a long time to be on Septra for a UTI. I'm surprised it's still working for her.

Hopefully she will get a good answer from her doctor.

Answer 5

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