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Simavastatin adverse events reported to FDA.

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Summary

FDA Adverse Reports: 11. View All

Simavastatin FDA safety alerts: No

Reported hospitalizations: 6

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

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6505088-X | Blood Pressure Increased, Dizziness, Fatigue, Hyperhidrosis, Influenza Like Illness, Musculoskeletal Stiffness
on Dec 04, 2009 Male patient from UNITED KINGDOM , 64 years of age, was diagnosed with blood cholesterol increased and was treated with Simavastatin (View Usage). Patient experienced the following unwanted or unexpected effects: blood pressure increased, dizziness (What is dizziness?), fatigue, hyperhidrosis, influenza like illness, musculoskeletal stiffness. Simavastatin dosage: 20 Mg. During the same period patient was treated with PRAVASTATIN SODIUM (40 Mg) (View Pravastatin Sodium Review and Pravastatin Sodium Label ).

6450474-X | Blood Creatine Phosphokinase Increased, Muscle Spasms
Patient was taking Simavastatin (View Usage). Patient had the following side effects: blood creatine phosphokinase increased, muscle spasms on Nov 20, 2009 from UNITED STATES Additional patient health information: Male patient , 74 years of age, weighting 168.0 lb, was diagnosed with hyperlipidaemia and. Simavastatin dosage: 20 Mg Every Day Po. Patient was hospitalized.

6445017-0 | Liver Disorder
Adverse event was reported on Oct 29, 2009 by a Male patient taking Simavastatin (View Usage) (Dosage: ) . Location: UNITED STATES , 63 years of age, After Simavastatin was administered, patient had the following side effects: liver disorder. Patient was hospitalized.

6434922-7 | Renal Failure Acute, Rhabdomyolysis
on Nov 09, 2009 Male patient from UNITED STATES , 53 years of age, weighting 253.0 lb, was diagnosed with diabetes mellitus, hyperlipidaemia and was treated with Simavastatin (View Usage). Patient experienced the following unwanted or unexpected effects: renal failure acute, rhabdomyolysis. Simavastatin dosage: 60 Mg Every Day Po; 600 Mg Bid Po. Patient was hospitalized.


6425970-1 | Balance Disorder, Fall, Renal Failure Acute, Rhabdomyolysis
on Nov 03, 2009 Female patient from UNITED STATES , 49 years of age, was diagnosed with hyperlipidaemia and was treated with Simavastatin (View Usage). Patient had the following side effects: balance disorder, fall (What is fall?), renal failure acute, rhabdomyolysis. Simavastatin dosage: 60 Mg Every Day Po.

6425968-3 | Hepatic Enzyme Increased, Rhabdomyolysis
Patient was taking Simavastatin (View Usage). After Simavastatin was administered, patient had the following side effects: hepatic enzyme increased, rhabdomyolysis on Nov 03, 2009 from UNITED STATES Additional patient health information: Male patient , 72 years of age, weighting 220.5 lb, . Simavastatin dosage: 80 Mg Hs Po. Patient was hospitalized.

6424906-7 | Hepatic Enzyme Increased, Renal Failure, Rhabdomyolysis
Adverse event was reported on Nov 02, 2009 by a Female patient taking Simavastatin (View Usage) (Dosage: 80 Mg Hs Po) was diagnosed with hyperlipidaemia and. Location: UNITED STATES , 78 years of age, Patient experienced the following unwanted or unexpected effects: hepatic enzyme increased, renal failure, rhabdomyolysis. Patient was hospitalized.

6424687-7 | Blood Urea Increased, Hepatic Enzyme Increased, Rhabdomyolysis
on Nov 02, 2009 Male patient from UNITED STATES , 78 years of age, weighting 149.9 lb, was diagnosed with hyperlipidaemia and was treated with Simavastatin (View Usage). Patient had the following side effects: blood urea increased, hepatic enzyme increased, rhabdomyolysis. Simavastatin dosage: 80 Mg Every Day Po. Patient was hospitalized.

6191240-2 | Influenza Like Illness
on May 13, 2009 Female patient from UNITED STATES , 61 years of age, weighting 130.0 lb, was diagnosed with blood cholesterol and was treated with Simavastatin (View Usage). After Simavastatin was administered, patient had the following side effects: influenza like illness. Simavastatin dosage: 40mg Once Daily By Mouth.

6179531-2 | Feeling Abnormal, Gait Disturbance
Patient was taking Simavastatin (View Usage). Patient experienced the following unwanted or unexpected effects: feeling abnormal, gait disturbance on May 01, 2009 from UNITED STATES Additional patient health information: Male patient , 51 years of age, weighting 225.0 lb, was diagnosed with blood cholesterol increased and. Simavastatin dosage: Half Pill At Bedtime Once A Day Po.

6029869-4 | Hepatic Enzyme Increased
Adverse event was reported on Jan 05, 2009 by a Male patient taking Simavastatin (View Usage) (Dosage: 40 Mg At Bedtime Po) was diagnosed with hyperlipidaemia and. Location: UNITED STATES , 83 years of age, weighting 151.0 lb, Patient had the following side effects: hepatic enzyme increased.


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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 Simavastatin 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 Simavastatin quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Simavastatin 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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Simavastatin Reactions
Balance Disorder
Blood Creatine Phosphokinase Increased
Blood Pressure Increased
Blood Urea Increased
DizzinessWhat is Dizziness?
FallWhat is Fall?
Fatigue
Feeling Abnormal
Gait Disturbance
Hepatic Enzyme Increased
Hyperhidrosis
Influenza Like Illness
Liver Disorder
Muscle Spasms
Musculoskeletal Stiffness
Renal Failure
Renal Failure Acute
Rhabdomyolysis
Simavastatin 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 Simavastatin 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!