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AMYOTROPHY side effect

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Voltaren Side Effects Report #5661580-1
Physician from FRANCE reported VOLTAREN problem on Mar 10, 2008. Female patient, 20 years of age, was diagnosed with pain and was treated with VOLTAREN. After drug was administered, patient experienced the following problems/side effects: amyotrophy, emergency care, exercise tolerance decreased, injection site abscess, necrotising fasciitis staphylococcal, staphylococcal abscess, surgery, . VOLTAREN dosage: 100 MG, QD. Patient was hospitalized and became disabled. Patient recovered.

Temodal Side Effects Report #5663434-3
TEMODAL problem was reported by a Physician from FRANCE on Mar 04, 2008. Female patient, 74 years of age, was diagnosed with glioblastoma, sepsis, urinary tract infection, fungal infection, prophylaxis and was treated with TEMODAL. After drug was administered, patient experienced the following problems/side effects: amyotrophy, aphasia, arthropathy, cholestasis, dehydration, disorientation, erysipelas, escherichia sepsis, escherichia urinary tract infection, . TEMODAL dosage: unknown. During the same period patient was treated with ROCEPHIN, AMIKACIN, CIPROFLOXACIN, BACTRIMTE, FLUCONAZOLE, FLAGYL, BRISTOPEN, MEDROL. Patient was hospitalized. Patient recovered.

Voltaren Side Effects Report #5675028-4
Physician from FRANCE reported VOLTAREN problem on Mar 17, 2008. Male patient, 20 years of age, weighting 158.7 lb, was diagnosed with pain and was treated with VOLTAREN. After drug was administered, patient experienced the following problems/side effects: amyotrophy, emergency care, exercise tolerance decreased, folliculitis, injection site abscess, necrotising fasciitis staphylococcal, staphylococcal abscess, surgery, . VOLTAREN dosage: 100 MG, QD. Patient was hospitalized and became disabled. Patient recovered.

Temodal Side Effects Report #5635872-6
TEMODAL problem was reported by a Physician from FRANCE on Feb 12, 2008. Female patient, 74 years of age, was diagnosed with glioblastoma, sepsis, urinary tract infection, fungal infection, prophylaxis and was treated with TEMODAL. After drug was administered, patient experienced the following problems/side effects: amyotrophy, aphasia, arthropathy, asthenia, blood alkaline phosphatase normal, cholestasis, dehydration, disorientation, erysipelas, . TEMODAL dosage: unknown. During the same period patient was treated with ROCEPHIN, AMIKIN, CIPROFLOXACIN, BACTRIMTE, FLUCONAZOLE, FLAGYL, BRISTOPEN, MEDROL. Patient was hospitalized. Patient recovered.


Lariam Side Effects Report #5588505-1
Physician from FRANCE reported LARIAM problem on Jan 02, 2008. Male patient, 61 years of age, was treated with LARIAM. After drug was administered, patient experienced the following problems/side effects: amyotrophy, upper motor neurone lesion, . LARIAM dosage: unknown. During the same period patient was treated with ENGERIX. Patient died on 10/22/2004.

Zophren Side Effects Report #5564975-X
ZOPHREN problem was reported by a Consumer or non-health professional from FRANCE on Dec 10, 2007. Male patient, 71 years of age, was diagnosed with prostate cancer and was treated with ZOPHREN. After drug was administered, patient experienced the following problems/side effects: amyotrophy, ataxia, extensor plantar response, fall, hyporeflexia, muscular weakness, neuropathy peripheral, paraesthesia, quadriparesis, . ZOPHREN dosage: unknown. During the same period patient was treated with TAXOTERE, NAVELBINE. Patient was hospitalized and became disabled. Patient recovered.

Valium Side Effects Report #5506629-1
Physician from FRANCE reported VALIUM problem on Oct 23, 2007. Male patient, 75 years of age, weighting 158.7 lb, was diagnosed with anxiety, somnolence and was treated with VALIUM. After drug was administered, patient experienced the following problems/side effects: amyotrophy, heart rate irregular, orthostatic hypotension, . VALIUM dosage: unknown. During the same period patient was treated with LAROXYL. Patient recovered.

Zevalin Side Effects Report #5524876-X
ZEVALIN problem was reported by a Physician from FRANCE on Nov 06, 2007. Male patient, 60 years of age, was diagnosed with bone marrow conditioning regimen and was treated with ZEVALIN. After drug was administered, patient experienced the following problems/side effects: amyotrophy, blood culture positive, blood ph increased, blood potassium decreased, blood pressure increased, dysaesthesia, electrocardiogram abnormal, encephalopathy, eschar, . ZEVALIN dosage: unknown. During the same period patient was treated with MABTHERA, CARMUSTINE, ETOPOSIDE, ARACYTINE, MELPHALAN, PROZAC, MOPRAL. Patient was hospitalized. Patient recovered.

Valium Side Effects Report #5483971-4
Physician from FRANCE reported VALIUM problem on Oct 02, 2007. Male patient, 76 years of age, was diagnosed with anxiety and was treated with VALIUM. After drug was administered, patient experienced the following problems/side effects: amyotrophy, . VALIUM dosage: unknown. During the same period patient was treated with LAROXYL. Patient recovered.


Velcade Side Effects Report #5468237-0
VELCADE problem was reported by a Health Professional from FRANCE on Sept 12, 2007. Male patient, 70 years of age, was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: amyotrophy, asthenia, dehydration, diarrhoea, neuropathy, pancytopenia, sensory disturbance, . VELCADE dosage: unknown. During the same period patient was treated with THALIDOMIDE, CORTISONE ACETATE. Patient was hospitalized. Patient recovered.

Tahor Side Effects Report #5432279-1
Physician from FRANCE reported TAHOR problem on Aug 22, 2007. Male patient, 53 years of age, was diagnosed with hypercholesterolaemia and was treated with TAHOR. After drug was administered, patient experienced the following problems/side effects: amyotrophy, blood creatine phosphokinase increased, muscle spasms, muscular weakness, myalgia, weight decreased, . TAHOR dosage: unknown. Patient recovered.

Lipitor Side Effects Report #5761690-4
LIPITOR problem was reported by a Physician from CHINA on June 01, 2008. Male patient, 65 years of age, weighting 132.3 lb, was diagnosed with coronary artery disease and was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: amyotrophy, blood creatine phosphokinase increased, muscular weakness, weight decreased, . LIPITOR dosage: unknown. Patient recovered.

Botox Side Effects Report #5767877-9
Physician from CANADA reported BOTOX problem on June 10, 2008. Female patient, weighting 136.7 lb, was treated with BOTOX. After drug was administered, patient experienced the following problems/side effects: amyotrophy, muscle disorder, pain, . BOTOX dosage: unknown. Patient recovered.

Botox Side Effects Report #5767901-3
BOTOX problem was reported by a Physician from CANADA on June 10, 2008. Female patient, weighting 136.7 lb, was treated with BOTOX. After drug was administered, patient experienced the following problems/side effects: amyotrophy, muscle disorder, pain, . BOTOX dosage: unknown. Patient recovered.


Zocor Side Effects Report #5730548-9
Physician from FRANCE reported ZOCOR problem on Apr 28, 2008. Female patient, 74 years of age, was diagnosed with dyslipidaemia and was treated with ZOCOR. After drug was administered, patient experienced the following problems/side effects: amyotrophy, dermatomyositis, erythema, myalgia, oedema, . ZOCOR dosage: unknown. Patient recovered.

Lipitor Side Effects Report #5734057-2
LIPITOR problem was reported by a Physician from CHINA on Apr 30, 2008. Male patient, 65 years of age, weighting 132.3 lb, was diagnosed with coronary artery disease and was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: amyotrophy, blood creatine phosphokinase increased, muscular weakness, weight decreased, . LIPITOR dosage: unknown. Patient recovered.

Verapamil Side Effects Report #5746008-5
Consumer or non-health professional from GERMANY reported VERAPAMIL BASICS problem on May 14, 2008. Female patient was diagnosed with angina pectoris, hearing impaired and was treated with VERAPAMIL BASICS. After drug was administered, patient experienced the following problems/side effects: amyotrophy, asthma, hearing impaired, myalgia, . VERAPAMIL BASICS dosage: 80 MG, TID. During the same period patient was treated with VERAPAMIL BASICS, HYDROCHLOROTHIAZIDE, DIGIMERCK. Patient recovered.

Verapamil Side Effects Report #5748910-7
VERAPAMIL BASICS problem was reported by a Consumer or non-health professional from GERMANY on May 20, 2008. Female patient was diagnosed with angina pectoris, hearing impaired and was treated with VERAPAMIL BASICS. After drug was administered, patient experienced the following problems/side effects: amyotrophy, asthma, hearing impaired, myalgia, . VERAPAMIL BASICS dosage: 80 MG, TID. During the same period patient was treated with VERAPAMIL BASICS, HYDROCHLOROTHIAZIDE, DIGIMERCK. Patient recovered.

Prograf Side Effects Report #5710529-1
Consumer or non-health professional from UNITED STATES reported PROGRAF problem on Apr 03, 2008. Male patient, 59 years of age, was diagnosed with liver transplant rejection, liver abscess and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: amyotrophy, anastomotic stenosis, bacteria stool identified, bile duct necrosis, cholangitis, clostridium difficile colitis, hepatic artery occlusion, hepatic artery thrombosis, liver abscess, . PROGRAF dosage: 2 MG, BID; 3 MG, BID. During the same period patient was treated with MYCOPHENOLATE MOFETIL, MYCOPHENOLATE MOFETIL, SIROLIMUS, ANTIBIOTICS, ACYCLOVIR. Patient was hospitalized. Patient recovered.


Zophren Side Effects Report #5711348-2
ZOPHREN problem was reported by a Consumer or non-health professional from FRANCE on Apr 08, 2008. Male patient, 71 years of age, was diagnosed with prostate cancer and was treated with ZOPHREN. After drug was administered, patient experienced the following problems/side effects: amyotrophy, ataxia, extensor plantar response, fall, hyporeflexia, muscular weakness, neuropathy peripheral, paraesthesia, quadriparesis, . ZOPHREN dosage: unknown. During the same period patient was treated with TAXOTERE, NAVELBINE. Patient was hospitalized and became disabled. Patient recovered.

Altace Side Effects Report #5294743-8
Consumer or non-health professional from FRANCE reported ALTACE problem on Apr 03, 2007. Female patient was diagnosed with essential hypertension, diabetes mellitus non-insulin-dependent, arthropathy, sleep disorder and was treated with ALTACE. After drug was administered, patient experienced the following problems/side effects: amyotrophy, dysarthria, facial palsy, hemiparesis, hypoglycaemia, poor peripheral circulation, . ALTACE dosage: 2.5 MG, QD. During the same period patient was treated with GLYBURIDE, DAFALGAN, LASILIX, NOCTRAN. Patient was hospitalized. Patient recovered.

Arimidex Side Effects Report #5296330-4
ARIMIDEX problem was reported by a Consumer or non-health professional from FRANCE on Apr 03, 2007. Female patient, 73 years of age, was diagnosed with breast cancer female and was treated with ARIMIDEX. After drug was administered, patient experienced the following problems/side effects: amyotrophy, asthenia, dizziness, myalgia, . ARIMIDEX dosage: unknown. Patient recovered.

Tahor Side Effects Report #5310695-6
Physician from FRANCE reported TAHOR problem on Apr 16, 2007. Male patient, 57 years of age, was diagnosed with hypercholesterolaemia and was treated with TAHOR. After drug was administered, patient experienced the following problems/side effects: amyotrophy, muscular weakness, myalgia, . TAHOR dosage: unknown. During the same period patient was treated with CRESTOR. Patient recovered.

Altace Side Effects Report #5275694-1
ALTACE problem was reported by a Consumer or non-health professional from FRANCE on Mar 15, 2007. Female patient was diagnosed with essential hypertension, diabetes mellitus non-insulin-dependent, arthropathy, sleep disorder and was treated with ALTACE. After drug was administered, patient experienced the following problems/side effects: amyotrophy, dysarthria, facial palsy, hemiparesis, hypoglycaemia, poor peripheral circulation, . ALTACE dosage: 2.5 MG, QD. During the same period patient was treated with GLYBURIDE, DAFALGAN, LASILIX, NOCTRAN. Patient was hospitalized. Patient recovered.

Augmentin Side Effects Report #5677172-4
Consumer or non-health professional from FRANCE reported AUGMENTIN problem on Mar 13, 2008. Female patient, 14 years of age, was diagnosed with productive cough and was treated with AUGMENTIN. After drug was administered, patient experienced the following problems/side effects: allergic bronchitis, amyotrophy, asthenia, asthma, cheilitis, conjunctival disorder, dry eye, dry mouth, dysgraphia, . AUGMENTIN dosage: unknown. During the same period patient was treated with ADVIL, EXOMUC, SOLUPRED, TUSSISEDAL, SPASFON LYOC. Patient was hospitalized and became disabled. Patient recovered.

Paxil Side Effects Report #5477215-7
PAXIL problem was reported by a Physician from JAPAN on Oct 02, 2007. Male patient, weighting 138.9 lb, was diagnosed with depression, hepatitis c and was treated with PAXIL. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, amyotrophy, antidiuretic hormone abnormality, blood sodium increased, dizziness, dysuria, encephalitis, headache, hyponatraemia, . PAXIL dosage: 10MG PER DAY. During the same period patient was treated with ZOLPIDEM, RIBAVIRIN, REBETOL, ROHYPNOL. Patient was hospitalized. Patient recovered.

Paxil Side Effects Report #5483800-9
Physician from JAPAN reported PAXIL problem on Oct 10, 2007. Male patient, weighting 138.9 lb, was diagnosed with depression, hepatitis c and was treated with PAXIL. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, amyotrophy, antidiuretic hormone abnormality, blood sodium increased, dizziness, dysuria, encephalitis, headache, hyponatraemia, . PAXIL dosage: 10MG PER DAY. During the same period patient was treated with ZOLPIDEM, RIBAVIRIN, REBETOL, ROHYPNOL. Patient was hospitalized. Patient recovered.

Paxil Side Effects Report #5486766-0
PAXIL problem was reported by a Physician from JAPAN on Oct 10, 2007. Male patient, 63 years of age, weighting 138.9 lb, was diagnosed with depression, hepatitis c and was treated with PAXIL. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, amyotrophy, anorexia, blood creatine phosphokinase increased, depressed level of consciousness, discomfort, disorientation, dizziness, dizziness postural, . PAXIL dosage: 10MG PER DAY. During the same period patient was treated with PEGINTERFERON ALFA, REBETOL, ROHYPNOL, ZOLPIDEM. Patient was hospitalized. Patient recovered.

Paxil Side Effects Report #5781910-X
Health Professional from JAPAN reported PAXIL problem on June 12, 2008. Male patient, 63 years of age, weighting 138.9 lb, was diagnosed with depression, hepatitis c and was treated with PAXIL. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, amyotrophy, anorexia, antidiuretic hormone abnormality, blood creatine phosphokinase increased, discomfort, disorientation, dizziness, dizziness postural, . PAXIL dosage: 10MG PER DAY. During the same period patient was treated with PEGINTERFERON ALFA, REBETOL, ROHYPNOL, MYSLEE. Patient was hospitalized. Patient recovered.

Augmentin Side Effects Report #5739158-0
AUGMENTIN problem was reported by a Physician from FRANCE on Mar 13, 2008. Female patient, 14 years of age, was diagnosed with productive cough and was treated with AUGMENTIN. After drug was administered, patient experienced the following problems/side effects: allergic bronchitis, amyotrophy, asthenia, asthma, cheilitis, conjunctival disorder, dry eye, dry mouth, dysgraphia, . AUGMENTIN dosage: unknown. During the same period patient was treated with ADVIL, EXOMUC, SOLUPRED, TUSSISEDAL, SPASFON LYOC. Patient was hospitalized and became disabled. Patient recovered.

Risperdal Side Effects Report #5721407-6
Physician from FRANCE reported RISPERDAL problem on Apr 25, 2008. Female patient, weighting 66.14 lb, was diagnosed with agitation, temporal arteritis, hypertension, insomnia and was treated with RISPERDAL. After drug was administered, patient experienced the following problems/side effects: abasia, accidental overdose, amyotrophy, aphasia, decubitus ulcer, dyspnoea, eating disorder, feeding disorder, . RISPERDAL dosage: unknown. During the same period patient was treated with GALANTAMINE HYDROBROMIDE, PREDNISONE, SOTALOL, SPASMINE. Patient was hospitalized. Patient recovered.