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Beractant adverse events reported to FDA.

Have You Experienced unusual Beractant symptoms? PatientsVille.com collects and analyzes Beractant side effect and adverse reports submitted by Beractant users, such as .

Summary

FDA Adverse Reports: 4. View All

Beractant FDA safety alerts: No

Reported deaths: 3

Reported hospitalizations: 4

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Often additional risks of using a medication, such as Beractant, 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 Beractant users, Learn more about unwanted side effects & find ways to reduce them. Browse Beractant Adverse Reports reported to FDA and participate in Beractant discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Beractant. 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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Beractant Adverse Effect Reports (FDA)

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6295328-7 | Acute Respiratory Distress Syndrome, Sclerema, Sepsis
on Jul 31, 2009 Male patient from INDIA , weighting 2.87 lb, was diagnosed with acute respiratory distress syndrome and was treated with Beractant (View Usage). Patient experienced the following unwanted or unexpected effects: acute respiratory distress syndrome, sclerema, sepsis (What is sepsis?). Beractant dosage: Two Doses Of 5.2 Ml Administered At 48 Hours Of Life.. During the same period patient was treated with CLAVULANATE POTASSIUM (Not Reported) (View Clavulanate Potassium Review and Clavulanate Potassium Label ), AMOXICILLIN (Not Reported) (View Amoxicillin Review and Amoxicillin Label ), AMIKACIN (Not Reported) (View Amikacin Review and Amikacin Label ), CEFOPERAZONE SODIUM (Not Reported) (View Cefoperazone Sodium Review and Cefoperazone Sodium Label ), SULBACTAM (Not Reported) (View Sulbactam Review and Sulbactam Label ), DOPAMINE HCL (Not Reported) (View Dopamine Hcl Review and Dopamine Hcl Label ), DOBUTAMINE HCL (Not Reported) (View Dobutamine Hcl Review and Dobutamine Hcl Label ). Patient was hospitalized.

6286166-X | Acute Respiratory Distress Syndrome, Sclerema, Sepsis
Patient was taking Beractant (View Usage). Patient had the following side effects: acute respiratory distress syndrome, sclerema, sepsis (What is sepsis?) on Jul 24, 2009 from INDIA Additional patient health information: Male patient , weighting 2.87 lb, was diagnosed with acute respiratory distress syndrome and. Beractant dosage: Two Doses Of 5.2 Ml Administered At 48 Hours Of Life.. Patient was hospitalized.

6279268-5 | Acute Respiratory Distress Syndrome, Sclerema, Sepsis
Adverse event was reported on Jul 20, 2009 by a Male patient taking Beractant (View Usage) (Dosage: Two Doses At 48 Hours Of Life.) was diagnosed with acute respiratory distress syndrome and. Location: INDIA , weighting 2.87 lb, After Beractant was administered, patient had the following side effects: acute respiratory distress syndrome, sclerema, sepsis (What is sepsis?). Patient was hospitalized.

5912431-9 | Pneumonitis
on Oct 03, 2008 Female patient from INDIA , weighting 3.31 lb, was diagnosed with neonatal respiratory distress syndrome and was treated with Beractant (View Usage). Patient experienced the following unwanted or unexpected effects: pneumonitis. Beractant 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 Beractant 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 Beractant quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Beractant 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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Beractant Reactions
Acute Respiratory Distress Syndrome
Pneumonitis
Sclerema
SepsisWhat is Sepsis?
Beractant 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 Beractant 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!