Have You experienced a side effect?
and Vote

Yes, Severe
Yes, Moderate
Yes, Minor
No
Discuss Results
1.5 million people annually are harmed from drug errors. Side Effects Reported Today:

Don't Risk Your Health!
Ask a Health Expert Now


ARRHYTHMIA SUPRAVENTRICULAR side effect

What is ARRHYTHMIA SUPRAVENTRICULAR ?
Help Community - Describe Your Side Effect   Search FDA Side Effects   Ask Health Expert   ARRHYTHMIA SUPRAVENTRICULAR and Recently Reported Side Effects   ARRHYTHMIA SUPRAVENTRICULAR and 15 most Active Side Effect polls   ARRHYTHMIA SUPRAVENTRICULAR and featured health surveys   Substances toxic to Health   Recent Hospital reviews   Comments about Side Effects   Hospital Quality reviews   Homecare Quality reviews
Health Expert

A Health Expert wants to answer your question.

Please provide details below.



Drugs associated with ARRHYTHMIA SUPRAVENTRICULAR

ACTONEL  ALDURAZYME  AMBRISENTAN  AMLODIPINE  AVANDIA  AVASTIN  BEVACIZUMAB  BONIVA  BUSULFEX  CAMPATH  CAPECITABINE  CETIRIZINE  CETUXIMAB  CIALIS  CILOSTAZOL  DOXYLAMINE  FLUDARABINE  FOSAMAX  GLEEVEC  HUMIRA  IRINOTECAN  ISOPTIN  KINERET  LIDOCAINE  PROGRAF  PROPOFOL  REBIF  RITUXAN  ROSIGLITAZONE  SORAFENIB  SUTENT  TEMODAR  VELCADE  ZINNATECTABLE  


Temodar Side Effects Report #5651812-8
Physician from UNITED STATES reported TEMODAR problem on Feb 25, 2008. Female patient, 79 years of age, weighting 173.9 lb, was diagnosed with glioblastoma multiforme and was treated with TEMODAR. After drug was administered, patient experienced the following problems/side effects: arrhythmia supraventricular, atrial fibrillation, bone marrow failure, sick sinus syndrome, urinary tract infection, . TEMODAR dosage: 75 MG/M2;QD;PO; 150 MG/M2;QD;PO;200 MG/M2;QD;PO. During the same period patient was treated with VITAMIN CAP. Patient was hospitalized. Patient died on 07/15/2007.

Sutent Side Effects Report #5673681-2
SUTENT problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 10, 2008. Male patient, weighting 207.9 lb, was diagnosed with renal cancer metastatic and was treated with SUTENT. After drug was administered, patient experienced the following problems/side effects: arrhythmia supraventricular, dyspnoea, haemothorax, . SUTENT dosage: unknown. During the same period patient was treated with LOVENOX, HYTRIN, BENZONATATE, COMPAZINE, HYCODAN, SYNTHROID, BIAFINE. Patient was hospitalized. Patient recovered.

Campath Side Effects Report #5625684-1
Physician from UNITED STATES reported CAMPATH problem on Feb 05, 2008. Male patient, 39 years of age, weighting 176.4 lb, was diagnosed with acute lymphocytic leukaemia, infection prophylaxis, tumour lysis syndrome and was treated with CAMPATH. After drug was administered, patient experienced the following problems/side effects: arrhythmia supraventricular, cardiac valve disease, cognitive disorder, cough, dehydration, dyspnoea, endocarditis, gastrointestinal haemorrhage, haematoma, . CAMPATH dosage: unknown. During the same period patient was treated with METHOTREXATE, VINCRISTINE, ELSPAR, DEXAMETHASONE, BACTRIM DS, FAMCICLOVIR, ALLOPURINOL. Patient was hospitalized. Patient recovered.

Kineret Side Effects Report #5626104-3
KINERET problem was reported by a Health Professional from GERMANY on Jan 30, 2008. Female patient, weighting 174.2 lb, was diagnosed with polyarthritis and was treated with KINERET. After drug was administered, patient experienced the following problems/side effects: arrhythmia supraventricular, atrial fibrillation, cardiac valve replacement complication, dyspnoea, mitral valve incompetence, pyrexia, rheumatoid arthritis, . KINERET dosage: unknown. During the same period patient was treated with PREDNISOLONE, DICLOFENAC, DIGITOXIN, PANTOZOL, BELOC ZOK, MARCUMAR, CLEXANE, DURAGESIC. Patient was hospitalized. Patient died on 05/16/2007.


Sorafenib Side Effects Report #5582708-8
Physician from GERMANY reported SORAFENIB problem on Dec 10, 2007. Male patient, 65 years of age, weighting 147.7 lb, was treated with SORAFENIB. After drug was administered, patient experienced the following problems/side effects: arrhythmia supraventricular, atrial fibrillation, . SORAFENIB dosage: TOTAL DAILY DOSE: 800 MG UNIT DOSE: 200 MG. During the same period patient was treated with GEMCITABINE, CISPLATIN. Patient was hospitalized. Patient recovered.

Capecitabine Side Effects Report #5586996-3
CAPECITABINE problem was reported by a Physician from SWITZERLAND on Dec 31, 2007. Female patient was diagnosed with adenocarcinoma pancreas and was treated with CAPECITABINE. After drug was administered, patient experienced the following problems/side effects: arrhythmia supraventricular, diarrhoea, enterobacter sepsis, syncope, . CAPECITABINE dosage: unknown. During the same period patient was treated with GEMCITABINE, ELOXATIN. Patient was hospitalized. Patient died on 12/12/2007.

Capecitabine Side Effects Report #5604797-4
Physician from FRANCE reported CAPECITABINE problem on Jan 15, 2008. Female patient, 74 years of age, was treated with CAPECITABINE. After drug was administered, patient experienced the following problems/side effects: arrhythmia supraventricular, diarrhoea, enterobacter sepsis, syncope, . CAPECITABINE dosage: FORM: FILM COATED TABLET. STRENGTH: 150MG OR 500MG.. During the same period patient was treated with GEMCITABINE, OXALIPLATIN. Patient was hospitalized. Patient died on 12/12/2007.

Bevacizumab Side Effects Report #5554544-X
BEVACIZUMAB problem was reported by a Physician from UNITED KINGDOM on Dec 03, 2007. Female patient was diagnosed with breast cancer and was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: arrhythmia supraventricular, disease progression, dyspnoea, left ventricular failure, myocardial ischaemia, pleural effusion, . BEVACIZUMAB dosage: 10 MG/KG, DAYS 1+15. During the same period patient was treated with TAXOL. Patient was hospitalized. Patient recovered.

Cialis Side Effects Report #5557864-8
Physician from BELGIUM reported CIALIS problem on Nov 30, 2007. Male patient, weighting 185.2 lb, was diagnosed with hypertension, platelet aggregation, hyperlipidaemia and was treated with CIALIS. After drug was administered, patient experienced the following problems/side effects: arrhythmia supraventricular, ventricular tachycardia, . CIALIS dosage: unknown. During the same period patient was treated with COVERSYL, MARCUMAR, BURINEX, LIPITOR, ALDACTONE, CORDARONE, DAKAR. Patient was hospitalized. Patient recovered.


Capecitabine Side Effects Report #5565253-5
CAPECITABINE problem was reported by a Physician from SWITZERLAND on Dec 10, 2007. Female patient was diagnosed with adenocarcinoma pancreas and was treated with CAPECITABINE. After drug was administered, patient experienced the following problems/side effects: arrhythmia supraventricular, diarrhoea, pyrexia, syncope, . CAPECITABINE dosage: unknown. During the same period patient was treated with GEMCITABINE, ELOXATIN. Patient was hospitalized. Patient recovered.

Boniva Side Effects Report #5571062-3
Physician from BELGIUM reported BONIVA problem on Dec 14, 2007. Female patient, 55 years of age, weighting 110.2 lb, was diagnosed with hypertension and was treated with BONIVA. After drug was administered, patient experienced the following problems/side effects: arrhythmia supraventricular, . BONIVA dosage: unknown. During the same period patient was treated with CALCIUM NOS, ISOTEN. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5517570-2
SUTENT problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 02, 2007. Male patient, weighting 231.5 lb, was diagnosed with prostate cancer, pain and was treated with SUTENT. After drug was administered, patient experienced the following problems/side effects: arrhythmia supraventricular, . SUTENT dosage: unknown. During the same period patient was treated with TAXOTERE, PREDNISONE, EXCEDRIN, OXYCODONE. Patient recovered.

Fosamax Side Effects Report #5518986-0
Health Professional from UNITED STATES reported FOSAMAX problem on Nov 14, 2007. Female patient, 52 years of age, weighting 200.0 lb, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: arrhythmia supraventricular, dizziness, ventricular arrhythmia, . FOSAMAX dosage: unknown. Patient recovered.

Sutent Side Effects Report #5484665-1
SUTENT problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 03, 2007. Male patient, weighting 231.5 lb, was diagnosed with prostate cancer, pain and was treated with SUTENT. After drug was administered, patient experienced the following problems/side effects: arrhythmia supraventricular, . SUTENT dosage: unknown. During the same period patient was treated with TAXOTERE, PREDNISONE, EXCEDRIN, OXYCODONE. Patient recovered.


Doxylamine Side Effects Report #5492033-1
Physician from UNITED STATES reported DOXYLAMINE problem on Oct 18, 2007. Male patient, 62 years of age, weighting 156.0 lb, was diagnosed with insomnia and was treated with DOXYLAMINE. After drug was administered, patient experienced the following problems/side effects: arrhythmia supraventricular, atrial fibrillation, atrial tachycardia, extrasystoles, . DOXYLAMINE dosage: unknown. Patient recovered.

Lidocaine Side Effects Report #5449275-0
LIDOCAINE problem was reported by a Consumer or non-health professional from GERMANY on Sept 04, 2007. Female patient, weighting 92.59 lb, was diagnosed with neuralgia and was treated with LIDOCAINE. After drug was administered, patient experienced the following problems/side effects: arrhythmia supraventricular, cardiomegaly, carotid sinus syndrome, coronary artery disease, gastritis, loss of consciousness, pneumothorax, post procedural complication, sick sinus syndrome, . LIDOCAINE dosage: unknown. During the same period patient was treated with ERGOTAMINE TARTARATE W, CARBAMAEPINE, GABAPENTIN, MIANSERIN HYDROCHLORIDE, BROMAZEPAM, POTASSIUM CHLORIDE, TRIMETAZIDINE, RAMIPRIL. Patient was hospitalized. Patient recovered.

Velcade Side Effects Report #5453459-5
Health Professional from UNITED STATES reported VELCADE problem on Sept 04, 2007. Male patient, 48 years of age, was diagnosed with neoplasm and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: arrhythmia supraventricular, atrial fibrillation, atrial flutter, dizziness, fall, head injury, hypotension, syncope, . VELCADE dosage: 1.30 MG/M2, UNK, IV BOLUS. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5471965-4
SUTENT problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 17, 2007. Male patient, weighting 231.5 lb, was diagnosed with prostate cancer, pain and was treated with SUTENT. After drug was administered, patient experienced the following problems/side effects: arrhythmia supraventricular, . SUTENT dosage: unknown. During the same period patient was treated with TAXOTERE, EXCEDRIN, OXYCODONE, PREDNISON. Patient recovered.

Irinotecan Side Effects Report #5418667-8
Consumer or non-health professional from UNITED STATES reported IRINOTECAN problem on Aug 08, 2007. Male patient, weighting 218.3 lb, was diagnosed with glioblastoma multiforme and was treated with IRINOTECAN. After drug was administered, patient experienced the following problems/side effects: arrhythmia supraventricular, diarrhoea, hyperglycaemia, neutropenia, renal failure, thrombocytopenia, . IRINOTECAN dosage: DAILY DOSE:125MG/M2-FREQ:FREQUENCY: ON DAY 1, 8, 22, 29. During the same period patient was treated with TEMODAR, WARFARIN, LOTREL, LASIX, TOPROL, DECADRON, LIPITOR. Patient was hospitalized. Patient died on 08/02/2007.


Temodar Side Effects Report #5422608-7
TEMODAR problem was reported by a Physician from UNITED STATES on Aug 10, 2007. Female patient, 79 years of age, weighting 173.9 lb, was diagnosed with glioblastoma multiforme and was treated with TEMODAR. After drug was administered, patient experienced the following problems/side effects: arrhythmia supraventricular, atrial fibrillation, bone marrow failure, dyspnoea, nodal arrhythmia, palpitations, pancytopenia, sick sinus syndrome, urinary tract infection, . TEMODAR dosage: 75 MG/M2; QD; PO, 150 MG/M2; QD; PO, 200 MG/M2; QD; PO. During the same period patient was treated with VITAMIN CAP. Patient was hospitalized. Patient died on 07/15/2007.

Temodar Side Effects Report #5428479-7
Physician from UNITED STATES reported TEMODAR problem on Aug 22, 2007. Female patient, 79 years of age, weighting 173.9 lb, was diagnosed with glioblastoma multiforme and was treated with TEMODAR. After drug was administered, patient experienced the following problems/side effects: arrhythmia supraventricular, atrial fibrillation, bone marrow failure, dyspnoea, nodal arrhythmia, palpitations, pancytopenia, sick sinus syndrome, urinary tract infection, . TEMODAR dosage: 75 MG/M2; QD; PO, 150 MG/M2; QD; PO, 200 MG/M2; QD; PO. During the same period patient was treated with VITAMIN CAP. Patient was hospitalized. Patient died on 07/15/2007.

Cialis Side Effects Report #5440462-4
CIALIS problem was reported by a Physician from BELGIUM on Aug 21, 2007. Male patient, 74 years of age, was diagnosed with hypertension, platelet aggregation, hyperlipidaemia and was treated with CIALIS. After drug was administered, patient experienced the following problems/side effects: arrhythmia supraventricular, cardiac arrest, . CIALIS dosage: 20 MG, AS NEEDED. During the same period patient was treated with PERINDOPRIL ERBUMINE, MARCUMAR, BURINEX, LIPITOR. Patient was hospitalized. Patient recovered.

Irinotecan Side Effects Report #5441111-1
Consumer or non-health professional from UNITED STATES reported IRINOTECAN problem on Aug 24, 2007. Male patient, weighting 218.3 lb, was diagnosed with glioblastoma multiforme and was treated with IRINOTECAN. After drug was administered, patient experienced the following problems/side effects: arrhythmia supraventricular, asthenia, diarrhoea, hyperglycaemia, hypotension, leukopenia, neutropenia, renal failure acute, sepsis, . IRINOTECAN dosage: DAILY DOSE:125MG/M2-FREQ:ON DAY 1 OF 6-WEEK CYCLE. During the same period patient was treated with TEMODAR, WARFARIN, LOTREL, LASIX, TOPROL, DECADRON, LIPITOR. Patient was hospitalized. Patient died on 08/02/2007.

Amlodipine Side Effects Report #5760419-3
AMLODIPINE problem was reported by a Health Professional from UNITED KINGDOM on May 28, 2008. Male patient, 69 years of age, weighting 149.9 lb, was diagnosed with hypertension, pruritus, systemic candida, blood bicarbonate decreased, prophylaxis and was treated with AMLODIPINE. After drug was administered, patient experienced the following problems/side effects: arrhythmia supraventricular, atrial flutter, blood magnesium decreased, blood pressure decreased, haemoglobin decreased, . AMLODIPINE dosage: unknown. During the same period patient was treated with CETIRIZINE, AMBISOME, CALCICHEW, DARBEPOETIN ALFA, OMEPRAZOLE, BICARBONATE. Patient recovered.

Amlodipine Side Effects Report #5762054-X
Health Professional from UNITED KINGDOM reported AMLODIPINE problem on May 26, 2008. Male patient, 69 years of age, weighting 149.9 lb, was diagnosed with hypertension, pruritus, systemic candida and was treated with AMLODIPINE. After drug was administered, patient experienced the following problems/side effects: arrhythmia supraventricular, atrial flutter, blood pressure decreased, haemoglobin decreased, heart rate increased, hypomagnesaemia, . AMLODIPINE dosage: 5 MG, QD, ORAL. During the same period patient was treated with CETIRIZINE, AMBISOME, CALCICHEW, DARBEPOETIN ALFA, OMEPRAZOLE, BICARBONATE IN PLASTIC CONTAINER. Patient recovered.

Actonel Side Effects Report #5762158-1
ACTONEL problem was reported by a Physician from CANADA on May 22, 2008. Female patient, 69 years of age, was diagnosed with osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: arrhythmia supraventricular, . ACTONEL dosage: 35 MG ONCE WEEKLY, ORAL. During the same period patient was treated with VITAMINS, CALCIUM, SOTALOL. Patient was hospitalized. Patient recovered.

Cetirizine Side Effects Report #5765581-4
Health Professional from UNITED KINGDOM reported CETIRIZINE problem on May 27, 2008. Male patient, 69 years of age, weighting 149.9 lb, was diagnosed with pruritus, systemic candida, hypertension and was treated with CETIRIZINE. After drug was administered, patient experienced the following problems/side effects: arrhythmia supraventricular, atrial flutter, blood magnesium decreased, blood pressure decreased, haemoglobin decreased, . CETIRIZINE dosage: 10 MG 1/1 DAYS, ORAL. During the same period patient was treated with AMBISOME, AMLODIPINE, CALCICHEW, DARBEPOETIN ALFA, OMEPRAZOLE, CARBONATE. Patient recovered.

Cetirizine Side Effects Report #5776168-1
CETIRIZINE problem was reported by a Health Professional from UNITED KINGDOM on May 30, 2008. Male patient, 69 years of age, was diagnosed with pruritus, hypertension, systemic candida and was treated with CETIRIZINE. After drug was administered, patient experienced the following problems/side effects: arrhythmia supraventricular, atrial flutter, blood magnesium decreased, blood pressure decreased, haemoglobin decreased, heart rate increased, . CETIRIZINE dosage: 10 MG; DAILY; ORAL. During the same period patient was treated with AMLODIPINE, AMBISOME, CALCICHEW, DARBEPOETIN ALFA, OMEPRAZOLE, BICARBONATE. Patient recovered.

Amlodipine Side Effects Report #5782375-4
Health Professional from reported AMLODIPINE BESYLATE problem on June 05, 2008. Male patient, 69 years of age, was diagnosed with hypertension, pruritus and was treated with AMLODIPINE BESYLATE. After drug was administered, patient experienced the following problems/side effects: arrhythmia supraventricular, atrial flutter, blood pressure decreased, . AMLODIPINE BESYLATE dosage: 5 MG, QD; PO. During the same period patient was treated with CETIRIZINE, AMBISOME, CALCICHEW, DARBEPOETIN, OMEPRAZOLE, BICARBONATE. Patient recovered.

Propofol Side Effects Report #5731949-5
PROPOFOL problem was reported by a Pharmacist from UNITED STATES on Apr 30, 2008. Male patient was diagnosed with septic shock and was treated with PROPOFOL. After drug was administered, patient experienced the following problems/side effects: arrhythmia supraventricular, cardiogenic shock, rhabdomyolysis, . PROPOFOL dosage: 3 TO 4 MG/KG/HOUR. During the same period patient was treated with OMEPRAZOLE, TAZOCILLINE, FUROSEMIDE, REMIFENTANIL. Patient was hospitalized. Patient recovered.

Gleevec Side Effects Report #5738891-4
Physician from UNITED STATES reported GLEEVEC problem on May 15, 2008. Male patient, 70 years of age, weighting 266.0 lb, was diagnosed with gastrointestinal stromal tumour and was treated with GLEEVEC. After drug was administered, patient experienced the following problems/side effects: arrhythmia supraventricular, chest pain, sinus tachycardia, . GLEEVEC dosage: unknown. During the same period patient was treated with COREG, BENAZEPRIL HYDROCHLORIDE, TRIAMTERENE AND HYDROCHLOROTHIAZIDE. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5695007-0
SUTENT problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 24, 2008. Male patient, weighting 231.5 lb, was diagnosed with prostate cancer, pain and was treated with SUTENT. After drug was administered, patient experienced the following problems/side effects: arrhythmia supraventricular, . SUTENT dosage: unknown. During the same period patient was treated with TAXOTERE, PREDNISONE, EXCEDRIN, OXYCODONE. Patient recovered.

Rosiglitazone Side Effects Report #5700889-X
Physician from UNITED STATES reported ROSIGLITAZONE problem on Apr 08, 2008. Male patient, 88 years of age, weighting 170.2 lb, was diagnosed with blood cholesterol increased and was treated with ROSIGLITAZONE. After drug was administered, patient experienced the following problems/side effects: arrhythmia supraventricular, lung neoplasm, . ROSIGLITAZONE dosage: 8MG PER DAY. During the same period patient was treated with TOPROL, LIPITOR. Patient was hospitalized. Patient recovered.

Ambrisentan Side Effects Report #5713010-9
AMBRISENTAN problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 16, 2008. Female patient, weighting 295.1 lb, was diagnosed with pulmonary hypertension and was treated with AMBRISENTAN. After drug was administered, patient experienced the following problems/side effects: arrhythmia supraventricular, asthma, hypertension, sinusitis, upper respiratory tract infection, . AMBRISENTAN dosage: unknown. During the same period patient was treated with ALDACTONE, TOPROL, COUMADIN, METOLAZONE, COZAAR, LASIX. Patient was hospitalized. Patient recovered.

Bevacizumab Side Effects Report #5718967-8
Physician from UNITED KINGDOM reported BEVACIZUMAB problem on Apr 10, 2008. Male patient was diagnosed with colon cancer and was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: arrhythmia supraventricular, sinus tachycardia, syncope, thrombosis, . BEVACIZUMAB dosage: 5 MG/KG, Q2W. During the same period patient was treated with OXALIPLATIN, LEUCOVORIN CALCIUM. Patient was hospitalized. Patient recovered.

Avandia Side Effects Report #5723550-4
AVANDIA problem was reported by a Physician from CANADA on Apr 17, 2008. Female patient, 57 years of age, was treated with AVANDIA. After drug was administered, patient experienced the following problems/side effects: arrhythmia supraventricular, cardiac failure congestive, pericardial effusion, pericarditis, pleural effusion, . AVANDIA dosage: 4MG TWICE PER DAY. During the same period patient was treated with CELEBREX, IMOVANE, PAXIL. Patient recovered.

Humira Side Effects Report #5724918-2
Pharmacist from UNITED STATES reported HUMIRA problem on Apr 30, 2008. Male patient, weighting 189.6 lb, was diagnosed with crohn's disease and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: arrhythmia supraventricular, brain natriuretic peptide increased, breath sounds abnormal, chest pain, dyspnoea, heart rate increased, palpitations, pulmonary embolism, . HUMIRA dosage: 40 MG EVERY OTHER WEEK SQ PREADMISSION X 8-10 WEEKS --. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5364030-8
SUTENT problem was reported by a Consumer or non-health professional from UNITED STATES on June 08, 2007. Male patient, weighting 207.9 lb, was diagnosed with renal cancer metastatic and was treated with SUTENT. After drug was administered, patient experienced the following problems/side effects: arrhythmia supraventricular, dyspnoea, haemothorax, . SUTENT dosage: unknown. During the same period patient was treated with LOVENOX, HYTRIN, BENZONATATE, COMPAZINE, HYCODAN, SYNTHROID, BIAFINE. Patient was hospitalized. Patient recovered.

Cetuximab Side Effects Report #5322607-X
Health Professional from GERMANY reported CETUXIMAB problem on Apr 30, 2007. Female patient, 46 years of age, was diagnosed with rectal cancer and was treated with CETUXIMAB. After drug was administered, patient experienced the following problems/side effects: arrhythmia supraventricular, dizziness, dyspnoea, myocardial ischaemia, nausea, pneumonia, vomiting, . CETUXIMAB dosage: unknown. During the same period patient was treated with ELOXATIN, XELODA. Patient was hospitalized. Patient recovered.

Capecitabine Side Effects Report #5337035-0
CAPECITABINE problem was reported by a Physician from UNITED STATES on May 17, 2007. Male patient, 54 years of age, weighting 282.0 lb, was treated with CAPECITABINE. After drug was administered, patient experienced the following problems/side effects: arrhythmia supraventricular, hypertension, myocardial infarction, ventricular arrhythmia, . CAPECITABINE dosage: unknown. During the same period patient was treated with DOCETAXEL. Patient was hospitalized. Patient died on 08/24/2005.

Velcade Side Effects Report #5339648-9
Physician from UNITED STATES reported VELCADE problem on May 15, 2007. Female patient, 72 years of age, weighting 302.7 lb, was diagnosed with mantle cell lymphoma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: arrhythmia supraventricular, atrial fibrillation, nodal arrhythmia, . VELCADE dosage: 6.40 MG,. During the same period patient was treated with CYCLOPHOSPHAMIDE, DOXORUBICIN, PREDNISONE, RITUXIMAB, VINCRISTINE. Patient was hospitalized. Patient recovered.

Rebif Side Effects Report #5316345-7
REBIF problem was reported by a Physician from UNITED STATES on Apr 19, 2007. Female patient, 39 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: arrhythmia supraventricular, chest discomfort, . REBIF dosage: unknown. During the same period patient was treated with ASPIRIN, ACIPHEX. Patient recovered.

Avastin Side Effects Report #5266778-2
Physician from UNITED STATES reported AVASTIN problem on Mar 01, 2007. Female patient, weighting 123.5 lb, was diagnosed with non-small cell lung cancer and was treated with AVASTIN. After drug was administered, patient experienced the following problems/side effects: arrhythmia supraventricular, hypotension, nodal arrhythmia, supraventricular tachycardia, . AVASTIN dosage: 840 MG, Q3W, INTRAVENOUS. During the same period patient was treated with ALIMTA, ASPIRIN, BENADRYL, DEXAMETHASONE, FENTANYL CITRATE, FOLIC ACID, GRANISETRON, PROMETHAZINE. Patient was hospitalized. Patient recovered.

Prograf Side Effects Report #5661590-4
PROGRAF problem was reported by a Physician from JAPAN on Feb 19, 2008. Male patient, 59 years of age, was diagnosed with rheumatoid arthritis and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: alcoholic liver disease, arrhythmia supraventricular, atrial fibrillation, atrial flutter, electrocardiogram pq interval prolonged, gastritis, tachyarrhythmia, . PROGRAF dosage: 3 MG, UID/QD, ORAL. During the same period patient was treated with PREDNISOLONE, LOXONIN, MUCOSTA. Patient recovered.

Zinnatectable Side Effects Report #5601307-2
Consumer or non-health professional from FRANCE reported ZINNATECTABLE problem on Jan 14, 2008. Female patient, 74 years of age, was treated with ZINNATECTABLE. After drug was administered, patient experienced the following problems/side effects: anaphylactic shock, arrhythmia supraventricular, blood pressure decreased, circulatory collapse, haemodynamic instability, ventricular arrhythmia, ventricular fibrillation, . ZINNATECTABLE dosage: unknown. During the same period patient was treated with NIMBEX, TRASYLOL, SUFENTA, KETAMINE, DIPRIVAN. Patient was hospitalized. Patient died on 09/02/2007.

Irinotecan Side Effects Report #5413061-8
IRINOTECAN problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 08, 2007. Male patient, weighting 218.3 lb, was diagnosed with glioblastoma multiforme and was treated with IRINOTECAN. After drug was administered, patient experienced the following problems/side effects: adrenal insufficiency, arrhythmia supraventricular, atrial fibrillation, diarrhoea, hyperglycaemia, hypotension, pancytopenia, renal failure, renal failure acute, . IRINOTECAN dosage: DAILY DOSE:125MG/M2-FREQ:FREQUENCY: ON DAY 1, 8, 22, 29. During the same period patient was treated with TEMODAR, WARFARIN, LOTREL, LASIX, TOPROL, DECADRON, LIPITOR. Patient was hospitalized. Patient died on 08/02/2007.

Temodar Side Effects Report #5414758-6
Consumer or non-health professional from UNITED STATES reported TEMODAR problem on Aug 08, 2007. Male patient, 68 years of age, weighting 218.3 lb, was diagnosed with glioblastoma multiforme and was treated with TEMODAR. After drug was administered, patient experienced the following problems/side effects: adrenal insufficiency, arrhythmia supraventricular, asthenia, atrial fibrillation, dehydration, diarrhoea, hyperglycaemia, hypotension, neutropenia, . TEMODAR dosage: 200 MG/M2;QD;PO. During the same period patient was treated with IRINOTECAN, COUMADIN, LOTREL, LASIX, TOPROL, DECADRON SRC, LIPITOR. Patient was hospitalized. Patient died on 08/02/2007.

Irinotecan Side Effects Report #5429275-7
IRINOTECAN problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 27, 2007. Male patient, weighting 218.3 lb, was diagnosed with glioblastoma multiforme and was treated with IRINOTECAN. After drug was administered, patient experienced the following problems/side effects: adrenal insufficiency, arrhythmia supraventricular, asthenia, atrial fibrillation, blood pressure abnormal, clostridial infection, dehydration, diarrhoea, hyperglycaemia, . IRINOTECAN dosage: 125MG/M2, 80MG/M2 DAYS 1, 8 IV. During the same period patient was treated with TEMODAR, COUMADIN, LOTREL, LASIX, TOPROL, DECADRON, LIPITOR. Patient died on 08/02/2007.

Temodar Side Effects Report #5443089-3
Health Professional from UNITED STATES reported TEMODAR problem on Aug 24, 2007. Male patient, 68 years of age, weighting 218.3 lb, was diagnosed with glioblastoma multiforme and was treated with TEMODAR. After drug was administered, patient experienced the following problems/side effects: adrenal insufficiency, arrhythmia supraventricular, atrial fibrillation, clostridium difficile colitis, dehydration, hyperglycaemia, hypotension, pancytopenia, renal failure acute, . TEMODAR dosage: 200 MG/M2; QD; PO. During the same period patient was treated with IRINOTECAN, COUMADIN, LOTREL, LASIX, TOPROL, DECADRON, LIPITOR. Patient was hospitalized. Patient died on 08/02/2007.

Isoptin Side Effects Report #5443235-1
ISOPTIN problem was reported by a Physician from POLAND on Aug 15, 2007. Female patient, 15 years of age, was treated with ISOPTIN. After drug was administered, patient experienced the following problems/side effects: arrhythmia, arrhythmia supraventricular, body temperature decreased, bradycardia, cardiac output increased, echocardiogram abnormal, hyperglycaemia, hypokalaemia, . ISOPTIN dosage: unknown. Patient was hospitalized. Patient recovered.

Aldurazyme Side Effects Report #5390734-7
Physician from FRANCE reported ALDURAZYME problem on Oct 07, 2005. Female patient, 17 years of age, was diagnosed with mucopolysaccharidosis i and was treated with ALDURAZYME. After drug was administered, patient experienced the following problems/side effects: areflexia, arrhythmia supraventricular, cardiac disorder, cerebral atrophy, depressed level of consciousness, disease progression, dyspnoea exertional, escherichia sepsis, fluid retention, . ALDURAZYME dosage: 1 MG/KG 1XW;IV. Patient was hospitalized. Patient recovered.

PatientsVille.com does not provide medical advice, diagnosis or treatment. The information 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. We hope you found our information about ARRHYTHMIA SUPRAVENTRICULAR side effects helpful. 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. Thank you for visiting Patientsville.net. Hope you enjoyed finding information on medications and found answers to Your Questions about ARRHYTHMIA SUPRAVENTRICULAR