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FLUID INTAKE REDUCED side effect

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Triamterene Side Effects Report #5634178-9
Pharmacist from UNITED STATES reported TRIAMTERENE AND HYDROCHLOROTHIAZIDE problem on Feb 21, 2008. Female patient, 74 years of age, weighting 112.4 lb, was diagnosed with hypertension and was treated with TRIAMTERENE AND HYDROCHLOROTHIAZIDE. After drug was administered, patient experienced the following problems/side effects: fluid intake reduced, hyponatraemia, nausea, oral intake reduced, vomiting, . TRIAMTERENE AND HYDROCHLOROTHIAZIDE dosage: unknown. During the same period patient was treated with CRESTOR, INDERAL LA, SYNTHROID. Patient was hospitalized. Patient recovered.

Cetuximab Side Effects Report #5483350-X
CETUXIMAB problem was reported by a Physician from UNITED STATES on Oct 09, 2007. Male patient, weighting 136.7 lb, was diagnosed with neoplasm malignant and was treated with CETUXIMAB. After drug was administered, patient experienced the following problems/side effects: fluid intake reduced, laryngeal erythema, laryngeal oedema, localised oedema, neck pain, oral intake reduced, . CETUXIMAB dosage: 250MG/M2. During the same period patient was treated with TAXOL. Patient was hospitalized. Patient recovered.

Valproate Side Effects Report #5771642-6
Physician from UNITED STATES reported VALPROATE problem on May 28, 2008. Male patient, 21 years of age, was diagnosed with schizophrenia and was treated with VALPROATE. After drug was administered, patient experienced the following problems/side effects: fluid intake reduced, hyperhidrosis, muscle rigidity, neuroleptic malignant syndrome, rhabdomyolysis, salivary hypersecretion, unevaluable event, . VALPROATE dosage: 600 MG DAILY. During the same period patient was treated with ZOTEPINE, OLANZAPINE, QUETIAPINE FUMARATE, QUETIAPINE FUMARATE, RISPERIDONE, LITHIUM CARBONATE, LITHIUM CARBONATE. Patient was hospitalized. Patient recovered.

Valproate Side Effects Report #5778932-1
VALPROATE problem was reported by a Physician from UNITED STATES on June 11, 2008. Male patient, 21 years of age, was diagnosed with schizophrenia and was treated with VALPROATE. After drug was administered, patient experienced the following problems/side effects: fluid intake reduced, hyperhidrosis, muscle rigidity, neuroleptic malignant syndrome, rhabdomyolysis, salivary hypersecretion, unevaluable event, . VALPROATE dosage: 600 MG DAILY. During the same period patient was treated with LODOPIN, OLANZAPINE, QUETIAPINE FUMARATE, QUETIAPINE FUMARATE, RISPERIDONE, LITHIUM CARBONATE, LITHIUM CARBONATE. Patient was hospitalized. Patient recovered.


Valproate Side Effects Report #5795465-7
Physician from UNITED STATES reported VALPROATE problem on June 20, 2008. Male patient, 21 years of age, was diagnosed with schizophrenia and was treated with VALPROATE. After drug was administered, patient experienced the following problems/side effects: fluid intake reduced, hyperhidrosis, muscle rigidity, neuroleptic malignant syndrome, rhabdomyolysis, salivary hypersecretion, unevaluable event, . VALPROATE dosage: 600 MG DAILY. During the same period patient was treated with LODOPIN, OLANZAPINE, QUETIAPINE FUMARATE, QUETIAPINE FUMARATE, RISPERIDONE. Patient was hospitalized. Patient recovered.

Crest Side Effects Report #5734399-0
CREST PRO HEALTH MOUTHWASH NIGHT NORMAL PROCTOR problem was reported by a Consumer or non-health professional from UNITED STATES on May 08, 2008. Female patient, 39 years of age, weighting 159.0 lb, was diagnosed with dental plaque, gingivitis, prophylaxis and was treated with CREST PRO HEALTH MOUTHWASH NIGHT NORMAL PROCTOR. After drug was administered, patient experienced the following problems/side effects: fluid intake reduced, gingival disorder, gingival ulceration, jaw disorder, oral intake reduced, oral pain, stomatitis, . CREST PRO HEALTH MOUTHWASH NIGHT NORMAL PROCTOR dosage: unknown. During the same period patient was treated with CREST PRO HEALTH MOUTHWASH NIGHT NORMAL PROCTOR, CREST PRO HEALTH MOUTHWASH NIGHT NORMAL PROCTOR. Patient recovered.

Yasmin Side Effects Report #5752373-5
Consumer or non-health professional from BRAZIL reported YASMIN problem on Feb 22, 2008. Female patient, 28 years of age, weighting 123.5 lb, was diagnosed with oral contraception and was treated with YASMIN. After drug was administered, patient experienced the following problems/side effects: fluid intake reduced, metrorrhagia, nausea, pharyngitis, vulvovaginal burning sensation, . YASMIN dosage: unknown. Patient was hospitalized. Patient recovered.

Topiramate Side Effects Report #5361790-7
TOPIRAMATE problem was reported by a Physician from NETHERLANDS on June 07, 2007. Female patient, weighting 19.84 lb, was diagnosed with partial seizures, convulsion, pain and was treated with TOPIRAMATE. After drug was administered, patient experienced the following problems/side effects: fluid intake reduced, somnolence, . TOPIRAMATE dosage: unknown. During the same period patient was treated with VALPROIC ACID, VALPROIC ACID, PARACETAMOL, DEPAKENE, VIGABETRINE, STESOLID. Patient was hospitalized and became disabled. Patient recovered.

Vancomycin Side Effects Report #5314513-1
Health Professional from UNITED STATES reported VANCOMYCIN problem on May 01, 2007. Male patient, 46 years of age, was diagnosed with brain abscess and was treated with VANCOMYCIN. After drug was administered, patient experienced the following problems/side effects: fluid intake reduced, renal failure acute, . VANCOMYCIN dosage: 1500MG EVERY 12 HOURS. During the same period patient was treated with TICARCILLIN. Patient recovered.


Topiramate Side Effects Report #5334738-9
TOPIRAMATE problem was reported by a Physician from NETHERLANDS on Feb 07, 2007. Female patient, weighting 19.84 lb, was diagnosed with partial seizures, convulsion, pain and was treated with TOPIRAMATE. After drug was administered, patient experienced the following problems/side effects: fluid intake reduced, somnolence, . TOPIRAMATE dosage: unknown. During the same period patient was treated with VALPROIC ACID, VALPROIC ACID, PARACETAMOL, DEPAKENE, VIGABETRINE, STESOLID. Patient was hospitalized and became disabled. Patient recovered.

Mirtazapine Side Effects Report #5290630-X
Consumer or non-health professional from UNITED KINGDOM reported MIRTAZAPINE problem on Mar 27, 2007. Male patient, 84 years of age, was diagnosed with pruritus and was treated with MIRTAZAPINE. After drug was administered, patient experienced the following problems/side effects: fluid intake reduced, lethargy, renal failure, . MIRTAZAPINE dosage: unknown. During the same period patient was treated with ALPHADERM, ACETYLSALICYLIC ACID SRT, BETAMETHASONE, CLOBETASOL PROPIONATE, DIPYRIDAMOLE, HYDROXOCOBALAMIN, INDAPAMIDE, PERINDOPRIL ERBUMINE. Patient was hospitalized. Patient recovered.

Mirtazapine Side Effects Report #5291430-7
MIRTAZAPINE problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Mar 21, 2007. Male patient, 84 years of age, weighting 176.4 lb, was diagnosed with pruritus and was treated with MIRTAZAPINE. After drug was administered, patient experienced the following problems/side effects: fluid intake reduced, lethargy, renal failure, . MIRTAZAPINE dosage: unknown. During the same period patient was treated with ALPHADERM, ASPIRIN, BETNOVATE, CLOBETASOL PROPIONATE, DIPYRIDAMOLE, HYDROXOCOBALAMIN, INDAPAMIDE, PERINDOPRIL ERBUMINE. Patient was hospitalized. Patient recovered.

Sudafed Side Effects Report #5310927-4
Physician from UNITED STATES reported SUDAFED problem on Apr 26, 2007. Male patient, 65 years of age, weighting 140.0 lb, was diagnosed with multiple allergies, sinusitis and was treated with SUDAFED. After drug was administered, patient experienced the following problems/side effects: fluid intake reduced, inflammatory bowel disease, . SUDAFED dosage: 120MG TAB 1/DAY ORAL. Patient recovered.

Humira Side Effects Report #5632566-8
HUMIRA problem was reported by a Consumer or non-health professional from GERMANY on Feb 12, 2008. Male patient, weighting 160.9 lb, was diagnosed with rheumatoid arthritis, hypertension and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: bronchitis, fluid intake reduced, oedema peripheral, renal failure, right ventricular failure, . HUMIRA dosage: unknown. During the same period patient was treated with METHOTREXATE, INFLIXIMAB, OLMESARTAN, PREDNISOLONE, BISOPROLOL FUMARATE. Patient was hospitalized. Patient died on 09/26/2007.


Crestor Side Effects Report #5593345-3
Physician from JAPAN reported CRESTOR problem on Jan 08, 2008. Female patient, 50 years of age, weighting 143.3 lb, was diagnosed with hyperlipidaemia, hypertension, insomnia and was treated with CRESTOR. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, fluid intake reduced, myalgia, . CRESTOR dosage: unknown. During the same period patient was treated with CARDENALIN, MEILAX, NORVASC. Patient recovered.

Clarithromycin Side Effects Report #5555423-4
CLARITHROMYCIN problem was reported by a Physician from JAPAN on Dec 05, 2007. Female patient, child 6 years of age, was treated with CLARITHROMYCIN. After drug was administered, patient experienced the following problems/side effects: blood creatine phosphokinase increased, fluid intake reduced, laboratory test abnormal, oxygen saturation decreased, rhabdomyolysis, tachypnoea, . CLARITHROMYCIN dosage: unknown. During the same period patient was treated with CHERRY BARK, TIPEPIDINE HIBENZATE, CYPROHEPTADINE HYDROCHLORIDE, SALBUTAMOL SULPHATE, AMBROXOL HYDROCHLORIDE. Patient was hospitalized. Patient recovered.

Temsirolimus Side Effects Report #5568253-4
Physician from UNITED STATES reported TEMSIROLIMUS problem on Dec 11, 2007. Male patient, 69 years of age, weighting 440.9 lb, was diagnosed with multiple myeloma, nausea, vomiting and was treated with TEMSIROLIMUS. After drug was administered, patient experienced the following problems/side effects: decreased appetite, fluid intake reduced, lower respiratory tract infection, malaise, nausea, pneumonia, pyrexia, vomiting, . TEMSIROLIMUS dosage: 15 MG ON DAYS 1, 8, 22 AND 29 AND THEN EVERY 35 DAYS. During the same period patient was treated with ATORVASTATIN, HEPARIN, OXYCODONE, VALACYCLOVIR, PREDNISONE, ONDANSETRON HYDROCHLORIDE, ONDANSETRON HYDROCHLORIDE, METOPROLOL TARTRATE. Patient was hospitalized. Patient recovered.

Diclofenac Side Effects Report #5520454-7
DICLOFENAC problem was reported by a Physician from GERMANY on Nov 12, 2007. Male patient, 56 years of age, was diagnosed with acute myeloid leukaemia and was treated with DICLOFENAC. After drug was administered, patient experienced the following problems/side effects: ascites, fluid intake reduced, hepatic failure, multi-organ failure, nephropathy toxic, oedema, pneumonia fungal, renal failure acute, sepsis, . DICLOFENAC dosage: unknown. During the same period patient was treated with AMBISOME, LEVOFLOXACIN, LASIX, TRIAMTERENE AND HYDROCHLOROTHIAZIDE, ALLOPURINOL. Patient was hospitalized. Patient died on 11/11/2007.

Diclofenac Side Effects Report #5522991-8
Physician from GERMANY reported DICLOFENAC problem on Nov 16, 2007. Male patient, 56 years of age, was diagnosed with acute myeloid leukaemia and was treated with DICLOFENAC. After drug was administered, patient experienced the following problems/side effects: ascites, fluid intake reduced, hepatic failure, malignant neoplasm progression, multi-organ failure, nephropathy toxic, oedema, pneumonia fungal, renal failure acute, . DICLOFENAC dosage: unknown. During the same period patient was treated with AMBISOME, LEVOFLOXACIN, LASIX, TRIAMTERENE AND HYDROCHLOROTHIAZIDE, ALLOPURINOL. Patient was hospitalized. Patient died on 11/11/2007.


Betaseron Side Effects Report #5523976-8
BETASERON problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 20, 2007. Female patient, 38 years of age, was diagnosed with multiple sclerosis and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: fluid intake reduced, injection site bruising, injection site erythema, vomiting, . BETASERON dosage: unknown. Patient was hospitalized. Patient recovered.

Diclofenac Side Effects Report #5524495-5
Physician from GERMANY reported DICLOFENAC problem on Nov 16, 2007. Male patient, 56 years of age, was diagnosed with acute myeloid leukaemia and was treated with DICLOFENAC. After drug was administered, patient experienced the following problems/side effects: ascites, fluid intake reduced, hepatic failure, malignant neoplasm progression, multi-organ failure, nephropathy toxic, oedema, pneumonia fungal, renal failure acute, . DICLOFENAC dosage: unknown. During the same period patient was treated with AMBISOME, LEVOFLOXACIN, LASIX, TRIAMTERENE AND HYDROCHLOROTHIAZIDE, ALLOPURINOL. Patient was hospitalized. Patient died on 11/11/2007.

Diclofenac Side Effects Report #5524859-X
DICLOFENAC problem was reported by a Physician from GERMANY on Nov 22, 2007. Male patient, 56 years of age, was diagnosed with acute myeloid leukaemia and was treated with DICLOFENAC. After drug was administered, patient experienced the following problems/side effects: ascites, fluid intake reduced, hepatic failure, malignant neoplasm progression, multi-organ failure, nephropathy toxic, oedema, pneumonia fungal, renal failure acute, . DICLOFENAC dosage: unknown. During the same period patient was treated with AMBISOME, LEVOFLOXACIN, LASIX, TRIAMTERENE AND HYDROCHLOROTHIAZIDE, ALLOPURINOL. Patient was hospitalized. Patient died on 11/11/2007.

Velcade Side Effects Report #5524864-3
Physician from GERMANY reported VELCADE problem on Nov 07, 2007. Male patient, 33 years of age, weighting 160.9 lb, was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: dehydration, fluid intake reduced, infection, renal failure, tachycardia, . VELCADE dosage: 1.30 MG/M2, INTRAVENOUS. During the same period patient was treated with ADRIAMYCIN RDF, DEXAMETHASONE, OMEPRAZOLE, PREDNISONE, TACROLIMUS, ZOMETA. Patient was hospitalized. Patient recovered.

Clofarabine Side Effects Report #5528506-2
CLOFARABINE problem was reported by a Health Professional from UNITED KINGDOM on Nov 05, 2007. Male patient was diagnosed with acute myeloid leukaemia and was treated with CLOFARABINE. After drug was administered, patient experienced the following problems/side effects: catheter related infection, fluid intake reduced, nausea, oedema, palmar-plantar erythrodysaesthesia syndrome, renal impairment, sepsis, therapeutic agent toxicity, . CLOFARABINE dosage: 20 MG/M2 QD X 5 IV. During the same period patient was treated with DAUNORUBICIN. Patient died.

Diclofenac Side Effects Report #5530110-7
Physician from GERMANY reported DICLOFENAC problem on Nov 27, 2007. Male patient, 56 years of age, was diagnosed with acute myeloid leukaemia and was treated with DICLOFENAC. After drug was administered, patient experienced the following problems/side effects: ascites, fluid intake reduced, hepatic failure, malignant neoplasm progression, multi-organ failure, nephropathy toxic, oedema, pneumonia fungal, renal failure acute, . DICLOFENAC dosage: unknown. During the same period patient was treated with AMBISOME, LEVOFLOXACIN, LASIX, TRIAMTERENE AND HYDROCHLOROTHIAZIDE, ALLOPURINOL. Patient was hospitalized. Patient died on 11/11/2007.

Velcade Side Effects Report #5533898-4
VELCADE problem was reported by a Physician from GERMANY on Nov 20, 2007. Male patient, 33 years of age, weighting 160.9 lb, was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: dehydration, fluid intake reduced, infection, renal failure, tachycardia, . VELCADE dosage: 1.30 MG/M2, INTRAVENOUS. During the same period patient was treated with DOXORUBICIN, DEXAMETHASONE, OMEPRAZOLE, PREDNISONE, TACROLIMUS, ZOMETA. Patient was hospitalized. Patient recovered.

Byetta Side Effects Report #5575690-0
Consumer or non-health professional from UNITED STATES reported BYETTA problem on Sept 25, 2007. Female patient, 47 years of age, weighting 207.0 lb, was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, fluid intake reduced, nausea, vomiting, weight decreased, . BYETTA dosage: unknown. During the same period patient was treated with AMARYL, LEVEMIR. Patient recovered.

Humira Side Effects Report #5492559-0
HUMIRA problem was reported by a Consumer or non-health professional from GERMANY on Oct 17, 2007. Male patient, weighting 160.9 lb, was diagnosed with rheumatoid arthritis, hypertension and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: bronchitis, fluid intake reduced, oedema peripheral, renal failure, right ventricular failure, . HUMIRA dosage: unknown. During the same period patient was treated with METHOTREXATE, INFLIXIMAB, OLMESARTAN, PREDNISOLONE, BISOPROLOL FUMARATE. Patient was hospitalized. Patient died on 09/26/2007.

Lithium Side Effects Report #5493264-7
Pharmacist from UNITED STATES reported LITHIUM CARBONATE problem on Oct 22, 2007. Male patient, 75 years of age, was diagnosed with bipolar disorder, mania, hypertension and was treated with LITHIUM CARBONATE. After drug was administered, patient experienced the following problems/side effects: diarrhoea, fluid intake reduced, renal failure acute, therapeutic agent toxicity, . LITHIUM CARBONATE dosage: 900 MG EVERY DAY PO. During the same period patient was treated with LITHIUM CARBONATE, LISINOPRIL AND HYDROCHLOROTHIAZIDE. Patient was hospitalized. Patient recovered.

Lithium Side Effects Report #5494731-2
LITHIUM CARBONATE problem was reported by a Pharmacist from UNITED STATES on Oct 23, 2007. Male patient, 75 years of age, was diagnosed with bipolar i disorder, hypertension and was treated with LITHIUM CARBONATE. After drug was administered, patient experienced the following problems/side effects: diarrhoea, fluid intake reduced, renal failure acute, therapeutic agent toxicity, . LITHIUM CARBONATE dosage: 900MG EVERY DAY PO. During the same period patient was treated with LISINOPRIL AND HYDROCHLOROTHIAZIDE. Patient was hospitalized. Patient recovered.

Humira Side Effects Report #5464610-5
Consumer or non-health professional from GERMANY reported HUMIRA problem on Sept 13, 2007. Male patient, weighting 160.9 lb, was diagnosed with rheumatoid arthritis, hypertension and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: bronchitis, fluid intake reduced, oedema peripheral, renal failure, right ventricular failure, . HUMIRA dosage: unknown. During the same period patient was treated with METHOTREXATE, INFLIXIMAB, OLMESARTAN, PREDNISOLONE, BISOPROLOL. Patient was hospitalized. Patient recovered.

Micardis Side Effects Report #5467533-0
MICARDIS problem was reported by a Consumer or non-health professional from SWEDEN on Sept 20, 2007. Female patient, weighting 196.2 lb, was diagnosed with cardiovascular disorder, cerebrovascular accident prophylaxis and was treated with MICARDIS. After drug was administered, patient experienced the following problems/side effects: confusional state, fluid intake reduced, renal failure, . MICARDIS dosage: unknown. During the same period patient was treated with RAMIPRIL, METFORMIN, SIMVASTATIN, EPOETIN BETA, FOLIC ACID, CYAN COBALAMIN. Patient was hospitalized. Patient recovered.

Lapatinib Side Effects Report #5406048-2
Physician from SPAIN reported LAPATINIB problem on July 27, 2007. Female patient, 39 years of age, weighting 99.21 lb, was treated with LAPATINIB. After drug was administered, patient experienced the following problems/side effects: diarrhoea, fluid intake reduced, gastritis, oral intake reduced, . LAPATINIB dosage: 1250MG PER DAY. During the same period patient was treated with CAPECITABINE. Patient was hospitalized. Patient recovered.

Temozolomide Side Effects Report #5409551-4
TEMOZOLOMIDE problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 07, 2007. Female patient, weighting 110.2 lb, was treated with TEMOZOLOMIDE. After drug was administered, patient experienced the following problems/side effects: asthenia, fluid intake reduced, hyperglycaemia, hyponatraemia, vomiting, . TEMOZOLOMIDE dosage: 2200 MG. Patient was hospitalized. Patient recovered.

Lapatinib Side Effects Report #5416728-0
Physician from SPAIN reported LAPATINIB problem on Aug 13, 2007. Female patient, 39 years of age, weighting 99.21 lb, was treated with LAPATINIB. After drug was administered, patient experienced the following problems/side effects: diarrhoea, fluid intake reduced, gastritis, oral intake reduced, . LAPATINIB dosage: 1250MG PER DAY. During the same period patient was treated with CAPECITABINE. Patient was hospitalized. Patient recovered.

Simvastatin Side Effects Report #5385348-9
SIMVASTATIN problem was reported by a Consumer or non-health professional from UNITED ARAB EMIRATES on July 09, 2007. Male patient, 77 years of age, weighting 150.0 lb, was diagnosed with myocardial infarction and was treated with SIMVASTATIN. After drug was administered, patient experienced the following problems/side effects: fatigue, fluid intake reduced, myalgia, vomiting, . SIMVASTATIN dosage: unknown. Patient was hospitalized. Patient recovered.

Simvastatin Side Effects Report #5385348-9
Consumer or non-health professional from UNITED ARAB EMIRATES reported SIMVASTATIN problem on July 09, 2007. Male patient, 77 years of age, weighting 150.0 lb, was diagnosed with myocardial infarction and was treated with SIMVASTATIN. After drug was administered, patient experienced the following problems/side effects: fatigue, fluid intake reduced, myalgia, vomiting, . SIMVASTATIN dosage: unknown. Patient was hospitalized. Patient recovered.

Detrol Side Effects Report #5725471-X
DETROL LA problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 23, 2008. Female patient, weighting 110.0 lb, was diagnosed with pollakiuria and was treated with DETROL LA. After drug was administered, patient experienced the following problems/side effects: dysuria, fluid intake reduced, impaired self-care, . DETROL LA dosage: unknown. Patient recovered.

Flomax Side Effects Report #5729750-1
Consumer or non-health professional from UNITED STATES reported FLOMAX problem on Apr 09, 2008. Male patient, 94 years of age, was diagnosed with benign prostatic hyperplasia, clostridial infection, hypertension, atrial fibrillation, gout and was treated with FLOMAX. After drug was administered, patient experienced the following problems/side effects: anorexia, fluid intake reduced, vomiting projectile, . FLOMAX dosage: unknown. During the same period patient was treated with FLAGYL, LISINOPRIL, COUMADIN, ALLOPURINOL. Patient recovered.

Chantix Side Effects Report #5734499-5
CHANTIX problem was reported by a Consumer or non-health professional from UNITED STATES on May 08, 2008. Female patient, 64 years of age, weighting 112.0 lb, was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: agitation, fluid intake reduced, gingival pain, glossodynia, mouth ulceration, oral discomfort, oral intake reduced, . CHANTIX dosage: .5 MG. 2X/DAY PO. Patient recovered.

Warfarin Side Effects Report #5739723-0
Pharmacist from UNITED STATES reported WARFARIN problem on May 12, 2008. Female patient, 86 years of age, was diagnosed with urinary tract infection, fungal infection and was treated with WARFARIN. After drug was administered, patient experienced the following problems/side effects: contusion, fluid intake reduced, international normalised ratio increased, mouth haemorrhage, oral intake reduced, urinary tract infection, . WARFARIN dosage: 2MG DAILY PO. During the same period patient was treated with LEVOFLOXACIN, FLUCONAZOLE. Patient was hospitalized. Patient recovered.

Lithium Side Effects Report #5709038-5
LITHIUM CARBONATE problem was reported by a Pharmacist from UNITED STATES on Apr 16, 2008. Female patient, 37 years of age, weighting 158.7 lb, was diagnosed with bipolar disorder and was treated with LITHIUM CARBONATE. After drug was administered, patient experienced the following problems/side effects: dialysis, fluid intake reduced, mental status changes, renal failure acute, therapeutic agent toxicity, . LITHIUM CARBONATE dosage: 450MG AM, 625 MG PM DAILY PO CHRONIC. During the same period patient was treated with OMEPRAZOLE, TEGRETOL, KLONOPIN, NEURONTIN, SYNTHROID, SEROQUEL. Patient was hospitalized. Patient recovered.

Lapatinib Side Effects Report #5354090-2
Physician from SPAIN reported LAPATINIB problem on June 04, 2007. Female patient, 39 years of age, weighting 99.21 lb, was treated with LAPATINIB. After drug was administered, patient experienced the following problems/side effects: diarrhoea, fluid intake reduced, gastritis, oral intake reduced, . LAPATINIB dosage: 1250MG PER DAY. During the same period patient was treated with CAPECITABINE. Patient was hospitalized. Patient recovered.

Betaseron Side Effects Report #5332574-0
BETASERON problem was reported by a Consumer or non-health professional from UNITED STATES on May 11, 2007. Female patient, 38 years of age, was diagnosed with multiple sclerosis and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: fluid intake reduced, injection site bruising, injection site erythema, vomiting, . BETASERON dosage: unknown. Patient was hospitalized. Patient recovered.

Rebif Side Effects Report #5315995-1
Health Professional from UNITED STATES reported REBIF problem on Apr 18, 2007. Female patient, 46 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: dehydration, fluid intake reduced, nasopharyngitis, oral intake reduced, pneumonia, renal failure, . REBIF dosage: unknown. During the same period patient was treated with DEXAMETHASONE, LEVOTHYROXINE. Patient was hospitalized. Patient recovered.

Zithromac Side Effects Report #5276298-7
ZITHROMAC problem was reported by a Physician from JAPAN on Mar 14, 2007. Male patient, weighting 136.7 lb, was diagnosed with pharyngitis and was treated with ZITHROMAC. After drug was administered, patient experienced the following problems/side effects: diarrhoea, fluid intake reduced, haemolytic uraemic syndrome, inflammation, renal failure acute, skin exfoliation, viral infection, vomiting, . ZITHROMAC dosage: unknown. During the same period patient was treated with LOXONIN, TRANSAMIN, PREDONINE, ASCORBIC ACID, GASTER, ALFAROL, ACTONEL. Patient was hospitalized. Patient recovered.

Enalapril Side Effects Report #5283001-3
Pharmacist from UNITED STATES reported ENALAPRIL MALEATE problem on Mar 29, 2007. Male patient, 52 years of age, was diagnosed with hypertension and was treated with ENALAPRIL MALEATE. After drug was administered, patient experienced the following problems/side effects: face oedema, fluid intake reduced, lip oedema, pharyngolaryngeal pain, renal failure acute, . ENALAPRIL MALEATE dosage: 10MG BID PO. During the same period patient was treated with DOCUSATE, FERROUS SULPHATE, CHLORIDE, WARFARIN, DIPHENHYDRAMINE, METHYLPREDNISOLONE SUCCINATE, OMEPRAZOLE. Patient was hospitalized. Patient recovered.

Dipyrone Side Effects Report #5678053-2
DIPYRONE problem was reported by a Consumer or non-health professional from ISRAEL on Feb 26, 2008. Female patient, 16 years of age, was treated with DIPYRONE. After drug was administered, patient experienced the following problems/side effects: abdominal pain, flank pain, fluid intake reduced, renal failure acute, suicide attempt, vomiting, . DIPYRONE dosage: 400 MG;TABLET;ORAL;ONCE. Patient recovered.

Dipyrone Side Effects Report #5678055-6
Consumer or non-health professional from ISRAEL reported DIPYRONE problem on Feb 26, 2008. Female patient, 13 years of age, was diagnosed with dysmenorrhoea and was treated with DIPYRONE. After drug was administered, patient experienced the following problems/side effects: arthralgia, flank pain, fluid intake reduced, myalgia, renal failure acute, . DIPYRONE dosage: 5000 MG;DAILY. During the same period patient was treated with ACETAMINOPHEN. Patient was hospitalized. Patient recovered.

Levaquin Side Effects Report #5613925-6
LEVAQUIN problem was reported by a Physician from UNITED STATES on Jan 30, 2008. Male patient, weighting 204.0 lb, was diagnosed with chronic sinusitis, cough, pyrexia, hiv infection, herpes zoster, pain and was treated with LEVAQUIN. After drug was administered, patient experienced the following problems/side effects: anorexia, burning sensation, fluid intake reduced, gallbladder enlargement, hepatic cirrhosis, hepatomegaly, hypoaesthesia, joint crepitation, joint injury, . LEVAQUIN dosage: unknown. During the same period patient was treated with KALETRA, DIDANOSINE, ZIAGEN, ACYCLOVIR, MS CONTIN. Patient recovered.

Levaquin Side Effects Report #5618655-2
Physician from UNITED STATES reported LEVAQUIN problem on Jan 21, 2008. Male patient, weighting 204.0 lb, was diagnosed with chronic sinusitis, cough, pyrexia, hiv infection, herpes zoster, pain and was treated with LEVAQUIN. After drug was administered, patient experienced the following problems/side effects: anorexia, burning sensation, fluid intake reduced, gallbladder enlargement, hepatic cirrhosis, hepatomegaly, hypoaesthesia, joint crepitation, joint injury, . LEVAQUIN dosage: unknown. During the same period patient was treated with KALETRA, DIDANOSINE, ZIAGEN, ACYCLOVIR, MS CONTIN. Patient recovered.