Sufenta Side Effects

If You had Sufenta side effect, You are not alone. Other patients reported side effects.

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Sufenta adverse events reported to FDA.

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

Summary

FDA Adverse Reports: 2. View All

Sufenta FDA safety alerts: No

Reported hospitalizations: 1

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

4967635-9 | Abortion Induced, Coarctation Of The Aorta, Congenital Hand Malformation, Duodenal Atresia, Kidney Malformation, Multiple Congenital Abnormalities, Oesophageal Atresia, Oesophagobronchial Fistula
on Feb 03, 2006 Female patient from FRANCE , 29 years of age, was treated with Sufenta (View Usage). Patient experienced the following unwanted or unexpected effects: abortion induced, coarctation of the aorta, congenital hand malformation, duodenal atresia, kidney malformation, multiple congenital abnormalities, oesophageal atresia, oesophagobronchial fistula. Sufenta dosage: Duration: A Few Hours. During the same period patient was treated with TOPALGIC (Duration: A Few Hours) (View Topalgic Review and Topalgic Label ), THIOPENTAL SODIUM (Duration: A Few Hours) (View Thiopental Sodium Review and Thiopental Sodium Label ), NIMBEX (Duration: A Few Hours) (View Nimbex Review and Nimbex Label ), PERFALGAN (Duration: A Few Hours) (View Perfalgan Review and Perfalgan Label ).

4915753-3 | Abortion Induced
Patient was taking Sufenta (View Usage). Patient had the following side effects: abortion induced on Feb 03, 2006 from FRANCE Additional patient health information: Female patient , 29 years of age, . Sufenta dosage: Duration: A Few Hours. During the same period patient was treated with TOPALGIC (Duration: A Few Hours) (View Topalgic Review and Topalgic Label ), THIOPENTAL SODIUM (Duration: A Few Hours) (View Thiopental Sodium Review and Thiopental Sodium Label ), NIMBEX (Duration: A Few Hours) (View Nimbex Review and Nimbex Label ), PERFALGAN (Duration: A Few Hours) (View Perfalgan Review and Perfalgan Label ). 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 Sufenta 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 Sufenta quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Sufenta 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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SUFENTA Side Effects

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Sufenta adverse events reported to FDA.

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Sufenta Adverse Effect Reports (FDA)

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Abortion Induced
Coarctation Of The Aorta
Congenital Hand Malformation
Duodenal Atresia
Kidney Malformation
Multiple Congenital Abnormalities
Oesophageal Atresia
Oesophagobronchial Fistula

SUFENTA Side Effects

Compare, Review and Rank Sufenta Side Effects

View Safety Poll Results

View Effectivness Poll Results

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Detailed Reporting will help others get complete information and find alternative treatments to avoid or reduce side effects associated with it.

Ask patient community about Sufenta related health issues.

Sufenta adverse events reported to FDA.

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Search By Drug Names, Symptoms or a Health Condition

Sufenta Adverse Effect Reports (FDA)

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Sufenta Reactions