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Disoprivan adverse events reported to FDA.

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Summary

FDA Adverse Reports: 5. View All

Disoprivan FDA safety alerts: No

Reported hospitalizations: 3

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Often additional risks of using a medication, such as Disoprivan, become known after product is used by a larger number of patients, for a longer period of time, and by patients with different health characteristics from those studied before drug approval. This page allows You to Find answers and discuss health symptoms with other Disoprivan users, Learn more about unwanted side effects & find ways to reduce them. Browse Disoprivan Adverse Reports reported to FDA and participate in Disoprivan discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Disoprivan. You can also Post a question to users community or Ask a Doctor. PatientsVille.com is Your Complete Guide to all common, undocumented and undisclosed side effects associated with drugs and vaccines. Browse More Drug Reports Here: A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

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Disoprivan Adverse Effect Reports (FDA)

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5755941-X | Propofol Infusion Syndrome
on May 28, 2008 Female patient from GERMANY , 21 years of age, weighting 143.3 lb, was diagnosed with sedation, prophylaxis and was treated with Disoprivan (View Usage). Patient experienced the following unwanted or unexpected effects: propofol infusion syndrome. Disoprivan dosage: . During the same period patient was treated with SUFENTANIL CITRATE (View Sufentanil Citrate Review and Sufentanil Citrate Label ), NOREPINEPHRINE (0.005-0.1 Ug/kg/min) (View Norepinephrine Review and Norepinephrine Label ).

5657018-0 | Acute Pulmonary Oedema
Patient was taking Disoprivan (View Usage). Patient had the following side effects: acute pulmonary oedema on Feb 28, 2008 from GERMANY Additional patient health information: Male patient , 50 years of age, was diagnosed with anaesthesia and. Disoprivan dosage: . Patient was hospitalized.

4953091-3 | Blood Creatine Phosphokinase Increased
Adverse event was reported on Mar 13, 2006 by a Male patient taking Disoprivan (View Usage) (Dosage: ) . Location: GERMANY , weighting 630.5 lb, After Disoprivan was administered, patient had the following side effects: blood creatine phosphokinase increased. Patient was hospitalized.

4883355-3 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Gamma-glutamyltransferase Increased, Transaminases Increased
on Jan 09, 2006 Female patient from GERMANY , weighting 147.7 lb, was diagnosed with anaesthesia, varicose vein operation and was treated with Disoprivan (View Usage). Patient experienced the following unwanted or unexpected effects: alanine aminotransferase increased, aspartate aminotransferase increased, gamma-glutamyltransferase increased, transaminases increased. Disoprivan dosage: . During the same period patient was treated with NITROUS OXIDE WITH OXYGEN (View Nitrous Oxide With Oxygen Review and Nitrous Oxide With Oxygen Label ), SEVOFLURANE (Up To 1.4 Vol%) (View Sevoflurane Review and Sevoflurane Label ), ATROPINE (View Atropine Review and Atropine Label ), ALFENTANIL (View Alfentanil Review and Alfentanil Label ).


4842718-2 | Coma, Convulsion
on Sep 07, 2005 Male patient from GERMANY , weighting 132.3 lb, was treated with Disoprivan (View Usage). Patient had the following side effects: coma, convulsion. Disoprivan dosage: . Patient was hospitalized.


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To find out about documented side effects or safety concerns read either the drug label or the drug's package insert. You may also want to speak with your pharmacist or healthcare provider. All medicines have benefits and risks. The risks are the chances that something unwanted or unexpected could happen to you when you use them. You can protect yourself by searching summaries of recent safety alerts, adverse reports. Sometimes there are risks that only come to light after a medical product gets on the market and is used in a larger number of patients, for a longer period of time, and in patients whose health characteristics are different from those of the patients studied before approval.

Be aware of the following potential Disoprivan risks to be aware of: 1. Watch for any Serious adverse events, such as life-threatening situation, which can require an admission to hospital or longer-than-expected hospital stay, permanent disability, birth defect, miscarriage, stillbirth, or birth with serious disease requires medical care to prevent permanent damage
2. Any potential Disoprivan quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Disoprivan use error: mixing up products with similar drug names or packaging, taking wrong dose of a drug because of confusing dosing instructions on label
4. When applicable, Problems with different manufacturer of same medicine: not getting same results from a generic drug as a brand name drug, or from another generic

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Disoprivan Reactions
Acute Pulmonary Oedema
Alanine Aminotransferase Increased
Aspartate Aminotransferase Increased
Blood Creatine Phosphokinase Increased
Coma
Convulsion
Gamma-glutamyltransferase Increased
Propofol Infusion Syndrome
Transaminases Increased
Disoprivan Side Effects Notice - The material on this site is for informational purposes only, and is not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. PatientsVille.com does not provide medical advice, diagnosis or treatment. The information regarding Disoprivan adverse reports, reviews and polls contained on PatientsVille.com site has not been scientifically or otherwise verified as to a cause and effect relationship and cannot be used to estimate the incidence of adverse drug reactions or for establishing or changing of patient treatments. Thank you for visiting Patientsville.com!