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Regitine adverse events reported to FDA.

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Summary

FDA Adverse Reports: 4. View All

Regitine FDA safety alerts: No

Reported hospitalizations: 1

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

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6094601-5 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Caesarean Section, Liver Disorder, Premature Labour
on Feb 13, 2009 Female patient from JAPAN , weighting 101.4 lb, was diagnosed with phaeochromocytoma, uterine contractions abnormal and was treated with Regitine (View Usage). Patient experienced the following unwanted or unexpected effects: alanine aminotransferase increased, aspartate aminotransferase increased, caesarean section, liver disorder, premature labour. Regitine dosage: 150mg - 200mg. During the same period patient was treated with ONOACT (200mg - 2g) (View Onoact Review and Onoact Label ), MAGNESIUM SULFATE (View Magnesium Sulfate Review and Magnesium Sulfate Label ).

6094599-X | Premature Baby
Patient was taking Regitine (View Usage). Patient had the following side effects: premature baby on Feb 13, 2009 from JAPAN Additional patient health information: Female patient , weighting 2.34 lb, was diagnosed with phaeochromocytoma and. Regitine dosage: Maternal Dose: 150-200 Mg. During the same period patient was treated with ONOACT (Maternal Dose: 200mg-2g) (View Onoact Review and Onoact Label ).

6081020-0 | Premature Baby
Adverse event was reported on Feb 06, 2009 by a Female patient taking Regitine (View Usage) (Dosage: Maternal Dose: 150-200 Mg) was diagnosed with phaeochromocytoma and. Location: JAPAN , weighting 2.34 lb, After Regitine was administered, patient had the following side effects: premature baby. During the same period patient was treated with ONOACT (Maternal Dose: 200mg-2g) (View Onoact Review and Onoact Label ).

5501020-6 | Caesarean Section, Phaeochromocytoma Excision
on Oct 22, 2007 Female patient from JAPAN , 37 years of age, weighting 105.8 lb, was diagnosed with phaeochromocytoma and was treated with Regitine (View Usage). Patient experienced the following unwanted or unexpected effects: caesarean section, phaeochromocytoma excision. Regitine dosage: 18 Mg. During the same period patient was treated with TRANDATE (300 Mg/d) (View Trandate Review and Trandate Label ), INSULIN (View Insulin Review and Insulin 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 Regitine 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 Regitine quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Regitine 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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Regitine Reactions
Alanine Aminotransferase Increased
Aspartate Aminotransferase Increased
Caesarean Section
Liver Disorder
Phaeochromocytoma Excision
Premature Baby
Premature Labour
Regitine 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 Regitine 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!