User Reviews for Immune globulin intravenous

For Myasthenia Gravis: “I have had Gammagard for 5 months and suffered flu like symptoms for at lest 2 days after infusions. I had Octagam yesterday and today and have no symptoms except feel very tired. It seemed to be less irritating to the veins also. The fluid amount was doubled so it put less stress on my kidneys.”

For Polymyositis/Dermatomyositis: “I got the IVIG infusions for 5 hours a day 4 or 5 days a week every 3 months. I did 2 rounds and I felt so energetic the week after treatment was over. It also helped rid me of the muscle pain and a lot of the weakness. It was exhausting having to get through the week of infusions but when it was over I felt really good. Unfortunately my rheumatologist retired and moved so I’m waiting to see if my new Dr is going to have me back on the treatment. I highly recommend trying this if you haven’t already!”

Gammagard S/D (immune globulin intravenous) for Primary Immunodeficiency Syndrome: “First dose I had a hemolytic reaction with severe back pain headache hypertension BP was 200/120 . Change to Octogam for next infusion and slowed rate down to max of 50cc / hr have tolerated well. Have had a lot less infections since started IVIG”

For Myasthenia Gravis: “iVIG literally saved my life ... AND enabled me to transition off CONSIDERABLY more problematic drugs such as corticosteroids and immunosuppressives (which in all fairness under certain circumstances controlled symptoms COMPLETELY -- BUT frequently presented both acute severely lifestyle limiting side effects AND long term high probability severe side effects AND sometimes for short terms completely failed to control ANY symptoms acceptably). For maintenance purposes, however, the dosages currently specified as reduced "maintenance" do not work FOR ME yet to provide complete replacement for the otherwise less noxious and reasonably effective drug, Pyridostigmine. I know other patients for which it DOES, however, and am inclined to recommend it as the standard treatment of choice, which of course it is NOT because it is an expensive human distilled substance rather than a chemically formulated item, thus affecting both availability and distribution.”

For Anti NMDA Receptor Encephalitis: “I was diagnosed with ANMDARE early 2013 I had a reasonably quick diagnosis and was started on a course of octagam and prednisone and had a very fast recovery I can't tell doses etc because I don't remember much from that time, I'm currently laying in hospital being treated for a relapse on a dosage of 30g per day over 5 days and 1g per day prednisone for 3 days I'm in day 2 and already feel much better”

Privigen (immune globulin intravenous) for Primary Immunodeficiency Syndrome: “The only medication out of 6 IVIG I tried that gave me anaphylactic shock.”

Asceniv (immune globulin intravenous) for Primary Immunodeficiency Syndrome: “Previous drug gave me pressure in my head and chest they lowered the rate to 50. Still having it and my heart rate was high. Switched to here, much better experience. Let's keep it up woot woot!”

Privigen (immune globulin intravenous) for Primary Immunodeficiency Syndrome: “While I have only been on this medication, I feel so much better. I didn't become ill at all through the winter.”

Asceniv (immune globulin intravenous) for Primary Immunodeficiency Syndrome: “Feel great. Need fewer infusions. Based on research seems like a good immunuglobin option”

Panzyga (immune globulin intravenous): “Occasionally experienced mild headache, but mostly very tolerable infusion.”

Octagam (immune globulin intravenous) for Primary Immunodeficiency Syndrome: “After having 20 grs of Octagam I felt a little dizzy and a minor headache.”

Octagam (immune globulin intravenous): “At 10 gms. only a mild headache the day after”

For Myasthenia Gravis: “73 y.o. male. Affected 2 years ago with Myasthenia Gravis full blown within a few weeks. On celcept & mestinon. Approx. a year in I went through a course of treatments. No effect.”