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Rofecoxib adverse events reported to FDA.

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Summary

FDA Adverse Reports: 3. View All

Rofecoxib FDA safety alerts: 2002 2004 2005

Reported hospitalizations: 2

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

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4744980-3 | Acute Coronary Syndrome, Arteriospasm Coronary, Electrocardiogram St Segment Elevation, Hyperhomocysteinaemia
on Aug 02, 2005 Male patient from SOUTH AFRICA , 59 years of age, weighting 176.4 lb, was diagnosed with analgesic effect and was treated with Rofecoxib (View Usage). Patient experienced the following unwanted or unexpected effects: acute coronary syndrome, arteriospasm coronary, electrocardiogram st segment elevation, hyperhomocysteinaemia. Rofecoxib dosage: . During the same period patient was treated with VALDECOXIB (View Valdecoxib Review and Valdecoxib Label ). Patient was hospitalized.

4589343-9 | Angina Pectoris, Blood Cholesterol Increased, Blood Triglycerides Increased, Haematocrit Decreased, Haemoglobin Decreased, Joint Swelling, Low Density Lipoprotein Increased, Memory Impairment, Myocardial Ischaemia
Patient was taking Rofecoxib (View Usage). Patient had the following side effects: angina pectoris, blood cholesterol increased, blood triglycerides increased, haematocrit decreased, haemoglobin decreased, joint swelling, low density lipoprotein increased, memory impairment, myocardial ischaemia on Feb 03, 2005 from Additional patient health information: Male patient , 78 years of age, was diagnosed with neoplasm prophylaxis and. Rofecoxib dosage: 25 Mg/daily. During the same period patient was treated with OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ).

4578361-2 | Blood Creatinine Increased, Disease Progression
Adverse event was reported on Feb 02, 2005 by a Male patient taking Rofecoxib (View Usage) (Dosage: 25 Mg Po Daily) . Location: , 75 years of age, After Rofecoxib was administered, patient had the following side effects: blood creatinine increased, disease progression. During the same period patient was treated with LISINOPRIL (View Lisinopril Review and Lisinopril Label ), ATENOLOL (View Atenolol Review and Atenolol Label ), SERTRALINE (View Sertraline Review and Sertraline Label ), FLOMAX (View Flomax Review and Flomax 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 Rofecoxib 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 Rofecoxib quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Rofecoxib 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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During the same period patient was treated with ROFECOXIB (View Rofecoxib Review and Rofecoxib Label ), ACEBUTOLOL (View Acebutolol Review and Acebutolol Label ).<<<<

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During the same period patient was treated with ROFECOXIB (12.5-25 Mg Twice A Day) (View Rofecoxib Review and Rofecoxib Label ), ASPIRIN (View Aspirin Review and Aspirin ...<<<<

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Rofecoxib Reactions
Acute Coronary Syndrome
Angina Pectoris
Arteriospasm Coronary
Blood Cholesterol Increased
Blood Creatinine Increased
Blood Triglycerides Increased
Disease Progression
Electrocardiogram St Segment Elevation
Haematocrit Decreased
Haemoglobin Decreased
Hyperhomocysteinaemia
Joint Swelling
Low Density Lipoprotein Increased
Memory Impairment
Myocardial Ischaemia
Rofecoxib 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 Rofecoxib 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!