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Hemigoxine adverse events reported to FDA.

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Summary

FDA Adverse Reports: 4. View All

Hemigoxine FDA safety alerts: No

Reported hospitalizations: 4

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

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5208675-4 | Osteitis, Osteonecrosis, Pain In Jaw, Surgery, Tooth Disorder, Tooth Extraction, Toothache, Wound Debridement
on Jan 05, 2007 Male patient from FRANCE , 80 years of age, weighting 165.3 lb, was diagnosed with atrial fibrillation (What is atrial fibrillation?), multiple myeloma (What is multiple myeloma?) and was treated with Hemigoxine (View Usage). Patient experienced the following unwanted or unexpected effects: osteitis, osteonecrosis (What is osteonecrosis?), pain in jaw, surgery (What is surgery?), tooth disorder (What is tooth disorder?), tooth extraction, toothache, wound debridement. Hemigoxine dosage: . During the same period patient was treated with TANAKAN (View Tanakan Review and Tanakan Label ), ZOMETA (4 Mg Every 6 Weeks (15 Courses)) (View Zometa Review and Zometa Label ), AREDIA (90 Mg Every 6 Weeks (40 Courses)) (View Aredia Review and Aredia Label ), PREVISCAN (Unk, Unk) (View Previscan Review and Previscan Label ), EFFEXOR (Unk, Unk) (View Effexor Review and Effexor Label ). Patient was hospitalized and became disabled.

5177161-2 | Osteitis, Osteonecrosis, Pain In Jaw, Surgery, Tooth Disorder, Tooth Extraction, Toothache
Patient was taking Hemigoxine (View Usage). Patient had the following side effects: osteitis, osteonecrosis (What is osteonecrosis?), pain in jaw, surgery (What is surgery?), tooth disorder (What is tooth disorder?), tooth extraction, toothache on Dec 13, 2004 from FRANCE Additional patient health information: Male patient , 80 years of age, weighting 165.3 lb, was diagnosed with atrial fibrillation (What is atrial fibrillation?), multiple myeloma (What is multiple myeloma?) and. Hemigoxine dosage: . During the same period patient was treated with TANAKAN (View Tanakan Review and Tanakan Label ), ZOMETA (4 Mg Every 6 Weeks (15 Courses)) (View Zometa Review and Zometa Label ), AREDIA (90 Mg Every 6 Weeks (40 Courses)) (View Aredia Review and Aredia Label ), PREVISCAN (Unk, Unk) (View Previscan Review and Previscan Label ), EFFEXOR (Unk, Unk) (View Effexor Review and Effexor Label ). Patient was hospitalized and became disabled.

5162511-3 | Osteitis, Osteonecrosis, Pain In Jaw, Surgery, Tooth Disorder, Tooth Extraction, Toothache
Adverse event was reported on Dec 13, 2004 by a Male patient taking Hemigoxine (View Usage) (Dosage: ) was diagnosed with atrial fibrillation (What is atrial fibrillation?), multiple myeloma (What is multiple myeloma?) and. Location: FRANCE , 80 years of age, weighting 165.3 lb, After Hemigoxine was administered, patient had the following side effects: osteitis, osteonecrosis (What is osteonecrosis?), pain in jaw, surgery (What is surgery?), tooth disorder (What is tooth disorder?), tooth extraction, toothache. During the same period patient was treated with TANAKAN (View Tanakan Review and Tanakan Label ), ZOMETA (4 Mg Every 6 Weeks (15 Courses)) (View Zometa Review and Zometa Label ), AREDIA (90 Mg Every 6 Weeks (40 Courses)) (View Aredia Review and Aredia Label ), PREVISCAN (Unk, Unk) (View Previscan Review and Previscan Label ), EFFEXOR (Unk, Unk) (View Effexor Review and Effexor Label ). Patient was hospitalized and became disabled.

5088958-1 | Blood Bilirubin Increased, C-reactive Protein Increased, Gamma-glutamyltransferase Increased, Jaundice, White Blood Cell Count Increased
on Aug 21, 2006 Female patient from FRANCE , 83 years of age, was diagnosed with wound infection, dysthymic disorder, diabetes mellitus, myocardial ischaemia and was treated with Hemigoxine (View Usage). Patient experienced the following unwanted or unexpected effects: blood bilirubin increased, c-reactive protein increased, gamma-glutamyltransferase increased, jaundice (What is jaundice?), white blood cell count increased. Hemigoxine dosage: Unk. During the same period patient was treated with FUCIDINE CAP (View Fucidine Cap Review and Fucidine Cap Label ), MOPRAL (View Mopral Review and Mopral Label ), SEROPRAM (Unk) (View Seropram Review and Seropram Label ), LANTUS (Unk) (View Lantus Review and Lantus Label ), OFLOCET (Unk) (View Oflocet Review and Oflocet Label ), STILNOX (View Stilnox Review and Stilnox Label ), PLAVIX (Unk) (View Plavix Review and Plavix 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 Hemigoxine 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 Hemigoxine quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Hemigoxine 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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Hemigoxine Reactions
Blood Bilirubin Increased
C-reactive Protein Increased
Gamma-glutamyltransferase Increased
JaundiceWhat is Jaundice?
Osteitis
OsteonecrosisWhat is Osteonecrosis?
Pain In Jaw
SurgeryWhat is Surgery?
Tooth DisorderWhat is Tooth disorder?
Tooth Extraction
Toothache
White Blood Cell Count Increased
Wound Debridement
Hemigoxine 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 Hemigoxine 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!