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Zactima adverse events reported to FDA.

Have You Experienced unusual Zactima symptoms? PatientsVille.com collects and analyzes Zactima side effect and adverse reports submitted by Zactima users, such as fatigue, besoin de dormir, palpitaioons cardiaque entre|.

Summary

FDA Adverse Reports: 8. View All

Zactima FDA safety alerts: No

Reported deaths: 2

Reported hospitalizations: 7

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

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6937774-1 | Colonic Fistula, Escherichia Urinary Tract Infection, Fall, Gastrointestinal Fistula, Pneumaturia
on Aug 23, 2010 Male patient from UNITED STATES , 64 years of age, weighting 233.8 lb, was diagnosed with glioblastoma and was treated with Zactima (View Usage). Patient experienced the following unwanted or unexpected effects: colonic fistula, escherichia urinary tract infection, fall (What is fall?), gastrointestinal fistula, pneumaturia. Zactima dosage: 100 Mg, Qd, Po. During the same period patient was treated with GLUCOSAMINE (View Glucosamine Review and Glucosamine Label ), XEPPRA (View Xeppra Review and Xeppra Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ), OXYCODONE HCL (View Oxycodone Hcl Review and Oxycodone Hcl Label ), PRILOSEC (View Prilosec Review and Prilosec Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ), ZOFRAN (View Zofran Review and Zofran Label ). Patient was hospitalized.

6487193-X | Abasia, Cerebral Haemorrhage, Communication Disorder, Electrocardiogram Qt Prolonged, Fatigue, International Normalised Ratio Increased, Intracranial Haematoma, Middle Insomnia, Unresponsive To Stimuli
Patient was taking Zactima (View Usage). Patient had the following side effects: abasia, cerebral haemorrhage, communication disorder, electrocardiogram qt prolonged, fatigue, international normalised ratio increased, intracranial haematoma, middle insomnia, unresponsive to stimuli on Dec 09, 2009 from UNITED STATES Additional patient health information: Male patient , weighting 204.0 lb, was diagnosed with disease recurrence, glioblastoma multiforme and. Zactima dosage: 200 Mg Once Daily Po; 100 Mg Once Daily Po. During the same period patient was treated with KEPPRA (ANTI SEIZURE) (View Keppra (anti-seizure) Review and Keppra (anti-seizure) Label ), FLUOXITINE (DEPRESSION) (View Fluoxitine (depression) Review and Fluoxitine (depression) Label ), BACLOFEN (MUSCLE RELAXANT) (View Baclofen (muscle Relaxant) Review and Baclofen (muscle Relaxant) Label ), WARFARIN (ANTICOAGULANT) (View Warfarin (anticoagulant) Review and Warfarin (anticoagulant) Label ), ZOFRAN (PRN FOR NAUSEA) (View Zofran (prn For Nausea) Review and Zofran (prn For Nausea) Label ). Patient was hospitalized.

6023453-4 | Asthenia, Disease Progression, Neurological Decompensation, Peripheral Motor Neuropathy
Adverse event was reported on Dec 26, 2008 by a Male patient taking Zactima (View Usage) (Dosage: 300mg Qd Daily X 28 Days Po) was diagnosed with glioblastoma multiforme and. Location: UNITED STATES , weighting 141.3 lb, After Zactima was administered, patient had the following side effects: asthenia, disease progression, neurological decompensation, peripheral motor neuropathy. During the same period patient was treated with HYDREA (500mg Po Bid Bid X 28 Days Po) (View Hydrea Review and Hydrea Label ), GLEEVEC (400mg Qd Daily X 28 Days Po) (View Gleevec Review and Gleevec Label ), LAMICTAL (View Lamictal Review and Lamictal Label ), KEPPRA (View Keppra Review and Keppra Label ), VALTREX (View Valtrex Review and Valtrex Label ), COLACE (View Colace Review and Colace Label ), METAMUCIL (View Metamucil Review and Metamucil Label ), DECADRON (View Decadron Review and Decadron Label ).

6003586-9 | Asthenia, Disease Progression, Peripheral Motor Neuropathy
on Dec 12, 2008 Male patient from UNITED STATES , weighting 141.3 lb, was diagnosed with glioblastoma multiforme and was treated with Zactima (View Usage). Patient experienced the following unwanted or unexpected effects: asthenia, disease progression, peripheral motor neuropathy. Zactima dosage: 300mg Qd Daily X 28 Days Po. During the same period patient was treated with GLEEVEC (400mg Qd Daily X 28 Days Po) (View Gleevec Review and Gleevec Label ), HYDREA (500mg Po Bid Bid X 28 Days Po) (View Hydrea Review and Hydrea Label ), LAMICTAL (View Lamictal Review and Lamictal Label ), KEPPRA (View Keppra Review and Keppra Label ), VALTREX (View Valtrex Review and Valtrex Label ), COLACE (View Colace Review and Colace Label ), METAMUCIL (View Metamucil Review and Metamucil Label ), DECADRON (View Decadron Review and Decadron Label ). Patient was hospitalized.


6000210-6 | Asthenia, Disease Progression, Peripheral Motor Neuropathy
on Dec 11, 2008 Male patient from UNITED STATES , weighting 141.3 lb, was diagnosed with glioblastoma multiforme and was treated with Zactima (View Usage). Patient had the following side effects: asthenia, disease progression, peripheral motor neuropathy. Zactima dosage: 300mg Qd Daily X 28 Days Po. During the same period patient was treated with GLEEVEC (400mg Qd Daily X 28 Days Po) (View Gleevec Review and Gleevec Label ), HYDREA (500mg Po Bid Bid X 28 Days Po) (View Hydrea Review and Hydrea Label ), LAMICTAL (View Lamictal Review and Lamictal Label ), KEPPRA (View Keppra Review and Keppra Label ), VALTREX (View Valtrex Review and Valtrex Label ), COLACE (View Colace Review and Colace Label ), METAMUCIL (View Metamucil Review and Metamucil Label ), DECADRON (View Decadron Review and Decadron Label ). Patient was hospitalized.

5862765-1 | Confusional State, Diarrhoea, Disease Progression, Dizziness, Nausea, Postoperative Fever, Urinary Incontinence
Patient was taking Zactima (View Usage). After Zactima was administered, patient had the following side effects: confusional state, diarrhoea, disease progression, dizziness (What is dizziness?), nausea (What is nausea?), postoperative fever, urinary incontinence (What is urinary incontinence?) on Aug 27, 2008 from UNITED STATES Additional patient health information: Male patient , 40 years of age, weighting 172.0 lb, was diagnosed with glioblastoma multiforme and. Zactima dosage: Zactima300mg Qd. During the same period patient was treated with HYDROXYUREA (Hyroxyurea 500mg Bid) (View Hydroxyurea Review and Hydroxyurea Label ), GLEEVEC (500mg Bid) (View Gleevec Review and Gleevec Label ), LEXAPRO (View Lexapro Review and Lexapro Label ), DILANTIN (View Dilantin Review and Dilantin Label ). Patient was hospitalized.

5696577-9 | Convulsion, Hyponatraemia, Pyrexia
Adverse event was reported on Apr 04, 2008 by a Male patient taking Zactima (View Usage) (Dosage: 100mg Po Qd) was diagnosed with glioblastoma multiforme and. Location: UNITED STATES , 60 years of age, weighting 165.3 lb, Patient experienced the following unwanted or unexpected effects: convulsion, hyponatraemia, pyrexia. During the same period patient was treated with GLEEVEC (400mg Po Qd) (View Gleevec Review and Gleevec Label ), HYDROXYUREA (500mg Po Bid) (View Hydroxyurea Review and Hydroxyurea Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ), DECADRON (View Decadron Review and Decadron Label ), NEXIUM (View Nexium Review and Nexium Label ), KEPPRA (View Keppra Review and Keppra Label ). Patient was hospitalized.

5575031-9 | Bacteraemia, Bacterial Sepsis, Duodenal Ulcer, Gastric Ulcer, Hypotension, Leukopenia, Pancytopenia, Refusal Of Treatment By Relative, Respiratory Distress
on Dec 21, 2007 Male patient from UNITED STATES , 63 years of age, weighting 243.4 lb, was diagnosed with glioblastoma multiforme, brain oedema and was treated with Zactima (View Usage). Patient had the following side effects: bacteraemia, bacterial sepsis, duodenal ulcer, gastric ulcer, hypotension, leukopenia, pancytopenia, refusal of treatment by relative, respiratory distress. Zactima dosage: 200 Mg Qd Po. During the same period patient was treated with DECADRON (8 Mg Po Bid) (View Decadron Review and Decadron Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), ATENOLOL (View Atenolol Review and Atenolol Label ), ATOVAQUONE SUSPENSION (View Atovaquone Suspension Review and Atovaquone Suspension Label ), CARDURA (View Cardura Review and Cardura Label ), FOLIC ACID (View Folic Acid Review and Folic Acid Label ), KEPPRA (View Keppra Review and Keppra Label ), LANTUS (View Lantus Review and Lantus 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 Zactima 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 Zactima quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Zactima 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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Zactima Reactions
Abasia
Asthenia
Bacteraemia
Bacterial Sepsis
Cerebral Haemorrhage
Colonic Fistula
Communication Disorder
Confusional State
Convulsion
Diarrhoea
Disease Progression
DizzinessWhat is Dizziness?
Duodenal Ulcer
Electrocardiogram Qt Prolonged
Escherichia Urinary Tract Infection
FallWhat is Fall?
Fatigue
Gastric Ulcer
Gastrointestinal Fistula
Hyponatraemia
Hypotension
International Normalised Ratio Increased
Intracranial Haematoma
Leukopenia
Middle Insomnia
NauseaWhat is Nausea?
Neurological Decompensation
Pancytopenia
Peripheral Motor Neuropathy
Pneumaturia
Zactima 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 Zactima 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!