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Monicor adverse events reported to FDA.

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Summary

FDA Adverse Reports: 1. View All

Monicor FDA safety alerts: No

Reported hospitalizations: 1

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

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5080493-X | Asthenia, Bundle Branch Block, Cardiovascular Disorder, Cholelithiasis, Conduction Disorder, Dyspnoea, Muscular Weakness
on Jul 20, 2000 Female patient from FRANCE , 80 years of age, was diagnosed with ill-defined disorder, cardiac failure congestive and was treated with Monicor (View Usage). Patient experienced the following unwanted or unexpected effects: asthenia, bundle branch block, cardiovascular disorder, cholelithiasis, conduction disorder, dyspnoea, muscular weakness. Monicor dosage: . During the same period patient was treated with COVERSYL (View Coversyl Review and Coversyl Label ), VASTAREL (View Vastarel Review and Vastarel Label ), ASPIRIN (View Aspirin Review and Aspirin 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 Monicor 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 Monicor quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Monicor 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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How Did You Deal with Side Effects?

... Esomeprazole Label ), XATRAL (View Xatral Review and Xatral Label ), LORAZEPAM (View Lorazepam Review and Lorazepam Label ), MONICOR (View Monicor Review and Monicor Label ).

Omnic Side Effects - Complete Patient's Guide | User Reviews: Male patient, 63 years of age, was diagnosed |Dry Ejaculation|No Intention To Do Intercourse|Eye Sight ...

... Seropram Label ), TEMESTA (View Temesta Review and Temesta Label ), IMOVANE (View Imovane Review and Imovane Label ), MONICOR L.P. (View Monicor L.p. Review and Monicor L.p ...

During the same period patient was treated with CRESTOR (View Crestor Review and Crestor Label ), ALPRESS (View Alpress Review and Alpress Label ), MONICOR LP (View ...

... Zovirax Review and Zovirax Label ), DEPAKENE (View Depakene Review and Depakene Label ), KARDEGIC (View Kardegic Review and Kardegic Label ), MONICOR L.P. (View Monicor L.p ...

During the same period patient was treated with TENORMIN (View Tenormin Review and Tenormin Label ), MONICOR LP (View Monicor Lp Review and Monicor Lp Label ), ASPIRIN (View ...

During the same period patient was treated with MONICOR L.P. (20 Mg Daily) (View Monicor L.p. Review and Monicor L.p. Label ), LASIX (40 Mg Daily) (View Lasix Review and ...

During the same period patient was treated with MONICOR LP (View Monicor Lp Review and Monicor Lp Label ), OMIX (View Omix Review and Omix Label ). Patient was hospitalized.

During the same period patient was treated with AUGMENTIN '125' (1 G, Tid) (View Augmentin '125' Review and Augmentin '125' Label ), MONICOR L.P. (40 Mg/day) (View Monicor L ...

During the same period patient was treated with TAREG (View Tareg Review and Tareg Label ), MONICOR (View Monicor Review and Monicor Label ), VASTAREL (View Vastarel Review and ...

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Monicor Reactions
Asthenia
Bundle Branch Block
Cardiovascular Disorder
Cholelithiasis
Conduction Disorder
Dyspnoea
Muscular Weakness
Monicor 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 Monicor 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!