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Actimax adverse events reported to FDA.

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Summary

FDA Adverse Reports: 10. View All

Actimax FDA safety alerts: No

Reported deaths: 3

Reported hospitalizations: 6

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

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5314459-9 | Asthenia, Dysarthria, Dyspnoea, Glossodynia, Guillain-barre Syndrome, Hyporeflexia, Muscular Weakness, Rash Pruritic
on Apr 23, 2007 Male patient from GERMANY , 52 years of age, weighting 189.6 lb, was diagnosed with bronchitis (What is bronchitis?), rhinitis, unevaluable event, lung infection and was treated with Actimax (View Usage). Patient experienced the following unwanted or unexpected effects: asthenia, dysarthria, dyspnoea, glossodynia, guillain-barre syndrome (What is guillain-barre syndrome?), hyporeflexia, muscular weakness, rash pruritic. Actimax dosage: Total Daily Dose: 400 Mg Unit Dose: 400 Mg. During the same period patient was treated with L THYROX JOD HEXAL (LEVOTHYROXINE) (View L-thyrox Jod Hexal (levothyroxine) Review and L-thyrox Jod Hexal (levothyroxine) Label ), SINUPRET (View Sinupret Review and Sinupret Label ), PARACETAMOL (Unit Dose: 500 Mg) (View Paracetamol Review and Paracetamol Label ), ACC (Unit Dose: 300 Mg) (View Acc Review and Acc Label ), AVELOX (Total Daily Dose: 400 Mg Unit Dose: 400 Mg) (View Avelox Review and Avelox Label ), JODETTEN (View Jodetten Review and Jodetten Label ), RANITIDIN 300 (View Ranitidin 300 Review and Ranitidin 300 Label ), TAVOR 1 (View Tavor 1 Review and Tavor 1 Label ). Patient was hospitalized.

5313413-0 | Cardiac Failure, Pulmonary Oedema, Vascular Occlusion
Patient was taking Actimax (View Usage). Patient had the following side effects: cardiac failure, pulmonary oedema, vascular occlusion on Apr 24, 2007 from GERMANY Additional patient health information: Male patient , 70 years of age, was diagnosed with sinobronchitis and. Actimax dosage: . During the same period patient was treated with ROXITHROMYCIN (View Roxithromycin Review and Roxithromycin Label ), METOPROLOL SUCCINATE (View Metoprolol Succinate Review and Metoprolol Succinate Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ), ASPIRIN (View Aspirin Review and Aspirin Label ). Patient was hospitalized.

5293115-X | Cardiovascular Disorder, Nausea, Tremor
Adverse event was reported on Mar 22, 2007 by a Male patient taking Actimax (View Usage) (Dosage: Total Daily Dose: 400 Mg Unit Dose: 400 Mg) was diagnosed with bronchitis (What is bronchitis?) and. Location: GERMANY , 74 years of age, weighting 132.3 lb, After Actimax was administered, patient had the following side effects: cardiovascular disorder, nausea (What is nausea?), tremor.

5285898-X | Cardiac Failure, Vascular Occlusion
on Mar 29, 2007 Male patient from GERMANY , 70 years of age, was diagnosed with sinobronchitis and was treated with Actimax (View Usage). Patient experienced the following unwanted or unexpected effects: cardiac failure, vascular occlusion. Actimax dosage: . During the same period patient was treated with ROXITHROMYCIN (View Roxithromycin Review and Roxithromycin Label ), METOPROLOL SUCCINATE (View Metoprolol Succinate Review and Metoprolol Succinate Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ), ASPIRIN (View Aspirin Review and Aspirin Label ). Patient was hospitalized.


5245086-X | Dizziness, Hyperventilation, Paraesthesia
on Feb 15, 2007 Female patient from GERMANY , 31 years of age, weighting 152.1 lb, was diagnosed with bronchitis (What is bronchitis?) and was treated with Actimax (View Usage). Patient had the following side effects: dizziness (What is dizziness?), hyperventilation, paraesthesia. Actimax dosage: Total Daily Dose: 400 Mg Unit Dose: 400 Mg. During the same period patient was treated with MUCOLYTICS (View Mucolytics Review and Mucolytics Label ).

5240793-7 | Anxiety, Asthenia, Cough, Dysarthria, Dyskinesia, Dyspnoea, Erythema
Patient was taking Actimax (View Usage). After Actimax was administered, patient had the following side effects: anxiety (What is anxiety?), asthenia, cough, dysarthria, dyskinesia, dyspnoea, erythema on Feb 14, 2007 from GERMANY Additional patient health information: Male patient , 52 years of age, weighting 189.6 lb, was diagnosed with bronchitis (What is bronchitis?), rhinitis and. Actimax dosage: Total Daily Dose: 400 Mg Unit Dose: 400 Mg. During the same period patient was treated with L THYROX JOD HEXAL (LEVOTHYROXINE) (View L-thyrox Jod Hexal (levothyroxine) Review and L-thyrox Jod Hexal (levothyroxine) Label ), SINUPRET (View Sinupret Review and Sinupret Label ). Patient was hospitalized.

5218893-7 | Angina Pectoris
Adverse event was reported on Jan 15, 2007 by a Male patient taking Actimax (View Usage) (Dosage: Total Daily Dose: 400 Mg Unit Dose: 400 Mg) was diagnosed with bronchitis (What is bronchitis?) and. Location: GERMANY , 39 years of age, weighting 187.4 lb, Patient experienced the following unwanted or unexpected effects: angina pectoris. During the same period patient was treated with BERODUAL N (View Berodual N Review and Berodual N Label ).

5157101-2 | Anxiety, Asthenia, Dysarthria, Dyspnoea, Glossodynia, Guillain-barre Syndrome, Hypotonia
on Nov 20, 2006 Male patient from GERMANY , 52 years of age, weighting 189.6 lb, was diagnosed with bronchitis (What is bronchitis?), rhinitis and was treated with Actimax (View Usage). Patient had the following side effects: anxiety (What is anxiety?), asthenia, dysarthria, dyspnoea, glossodynia, guillain-barre syndrome (What is guillain-barre syndrome?), hypotonia. Actimax dosage: Total Daily Dose: 400 Mg Unit Dose: 400 Mg. During the same period patient was treated with L THYROX JOD HEXAL (LEVOTHYROXINE) (View L-thyrox Jod Hexal (levothyroxine) Review and L-thyrox Jod Hexal (levothyroxine) Label ), SINUPRET (View Sinupret Review and Sinupret Label ). Patient was hospitalized.

5150298-X | Dyspnoea, Erythema, Hypersensitivity
on Nov 02, 2006 Female patient from GERMANY , 54 years of age, weighting 165.3 lb, was diagnosed with bronchitis (What is bronchitis?) and was treated with Actimax (View Usage). After Actimax was administered, patient had the following side effects: dyspnoea, erythema, hypersensitivity. Actimax dosage: Total Daily Dose: 400 Mg Unit Dose: 400 Mg.

5085156-2 | Diabetes Mellitus Insulin-dependent
Patient was taking Actimax (View Usage). Patient experienced the following unwanted or unexpected effects: diabetes mellitus insulin-dependent on Jun 19, 2006 from GERMANY Additional patient health information: Male patient , 38 years of age, weighting 167.6 lb, was diagnosed with sinusitis (What is sinusitis?) and. Actimax dosage: Unit Dose: 400 Mg.


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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 Actimax 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 Actimax quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Actimax 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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Actimax Reactions
Angina Pectoris
AnxietyWhat is Anxiety?
Asthenia
Cardiac Failure
Cardiovascular Disorder
Cough
Diabetes Mellitus Insulin-dependent
DizzinessWhat is Dizziness?
Dysarthria
Dyskinesia
Dyspnoea
Erythema
Glossodynia
Guillain-barre SyndromeWhat is Guillain-barre syndrome?
Hypersensitivity
Hyperventilation
Hyporeflexia
Hypotonia
Muscular Weakness
NauseaWhat is Nausea?
Paraesthesia
Pulmonary Oedema
Rash Pruritic
Tremor
Vascular Occlusion
Actimax 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 Actimax 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!