FLUID RETENTION side effect
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Drugs associated with FLUID RETENTION
ABRAXANE ACETYLSALICYLIC ACTOS ADVAIR ALEVE ALKA ALKERAN AMLODIPINE ANGELIQ ARANESP ARIMIDEX ATACAND AVANDAMET AVANDIA AVASTIN AVONEX BETAFERON BETASERON BEXTRA BUMEX BYETTA CADUET CAMPATH CAMPRAL CAPTOPRIL CARDIZEM CARVEDILOL CELEBREX CEPHALEXIN CHAMPIX CHANTIX CIFLOX CIPROFLOXACIN CLIMARA CLOFARABINE CLOMIPHENE COMMIT COMPETACT COREG COUMADIN CRESTOR CYCLOSPORINE CYMBALTA DACOGEN DDAVP DECADRON DETROL DETRUSITOL DIANEAL DIGITEK DIGOXIN DILANTIN DILTIAZEM DIOVAN DIVALPROEX DURAGESIC EBIXA ELISOR ESTRADIOL EVICEL EVISTA EXENATIDE FABRAZYME FENTANYL FLOTAC FORTEO FOSAMAX FUROSEMIDE GEMCITABINE GEMTUZUMAB GEMZAR GLEEVEC GLUCOPHAGE GLYBURIDE HEPARIN HERCEPTIN HUMALOG HUMATE HUMIRA HUMULIN HYDROCHLOROTHIAZ HYZAAR IBUPROFEN IMATINIB INSULIN INVEGA JANUVIA KALETRA LAMICTAL LANTUS LETAIRIS LEVAQUIN LEVEMIR LEVETIRACETAM LEVOXYL LIORESAL LIPITOR LISINOPRIL LONOLOX LORAZEPAM LYRICA MEDROL MENOSTAR MERIDIA METFORMIN METHADONE MIRALAX MIRAPEX MIRENA MYFORTIC NAPROXEN NATALIZUMAB NEUMEGA NEUPRO NEURONTIN NEXIUM NIASPAN NICORETTE NORVASC NOVANTRONE NOVOLOG NOXAFIL NUTROPIN OLMESARTAN OMEPRAZOLE ORENCIA ORLISTAT ORTHO OSMOPREP PEGASYS PIOGLITAZONE PRAVASTATIN PREDNISONE PREMARIN PREMPRO PROCRIT PROGRAF PROLEUKIN PROZAC PULMICORT REBIF REMICADE REQUIP REVLIMID RHINADVIL RITUXAN ROCEPHIN ROSIGLITAZONE ROZEREM SANCTURA SANDOSTATIN SERETIDE SEROQUEL SILDENAFIL SPIRIVA SPORANOX SPRYCEL STARLIX STEROIDS SUBOXONE SUTENT SYMLIN TAMIFLU TAMOXIFEN TARKA TAXOTERE TEKTURNA TEMOZOLOMIDE THALOMID THYMOGLOBULIN TIKOSYN TOPROL TORSEMIDE TRACLEER TRILEPTAL TRUVADA VELCADE VESICARE VIAGRA VIANITE VIOXX VIREAD VISUDYNE VORICONAZOLE WELLBUTRIN XELODA ZELNORM ZOLADEX ZOMETA ZOVIRAX ZYPREXAActos Side Effects Report #5650700-0
Health Professional from UNITED STATES reported ACTOS problem on Mar 04, 2008. Female patient, 55 years of age, weighting 265.0 lb, was diagnosed with insulin resistance and was treated with ACTOS. After drug was administered, patient experienced the following problems/side effects: fluid retention, weight increased, . ACTOS dosage: unknown. Patient recovered.
Aleve Side Effects Report #5658879-1
ALEVE problem was reported by a Consumer or non-health professional from UNITED STATES on May 04, 2007. Male patient was diagnosed with osteoarthritis, cardiovascular event prophylaxis and was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: fluid retention, weight increased, . ALEVE dosage: UNIT DOSE: 220 MG. During the same period patient was treated with ECOTRIN, ACE INHIBITORS AND DIURETIC. Patient recovered.
Aleve Side Effects Report #5659070-5
Consumer or non-health professional from UNITED STATES reported ALEVE problem on Dec 18, 2007. Female patient, 80 years of age, weighting 110.2 lb, was diagnosed with analgesia and was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: fluid retention, . ALEVE dosage: UNIT DOSE: 220 MG. During the same period patient was treated with SINEMET. Patient recovered.
Aleve Side Effects Report #5659206-6
ALEVE problem was reported by a Consumer or non-health professional from UNITED STATES on June 11, 2007. Male patient, 72 years of age, weighting 136.7 lb, was diagnosed with arthritis and was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: fluid retention, . ALEVE dosage: UNIT DOSE: 220 MG. During the same period patient was treated with GLUCOPHAGE, TOPROL, PHENYTEK. Patient recovered.
Aleve Side Effects Report #5659300-X
Consumer or non-health professional from UNITED STATES reported ALEVE problem on June 25, 2007. Female patient, 73 years of age, weighting 209.4 lb, was diagnosed with back pain and was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: fluid retention, somnolence, . ALEVE dosage: UNIT DOSE: 220 MG. During the same period patient was treated with INSULIN, COZAAR, DEMADEX. Patient recovered.
Aleve Side Effects Report #5659825-7
ALEVE problem was reported by a Consumer or non-health professional from UNITED STATES on July 25, 2007. Female patient, 68 years of age, weighting 200.6 lb, was diagnosed with arthralgia and was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: fluid retention, . ALEVE dosage: UNIT DOSE: 220 MG. During the same period patient was treated with DIOVAN, SULFASALAZINE, TRIAMTERENE AND HYDROCHLOROTHIAZIDE. Patient recovered.
Aleve Side Effects Report #5660371-5
Consumer or non-health professional from UNITED STATES reported ALEVE problem on Oct 10, 2007. Male patient, weighting 244.7 lb, was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: fluid retention, . ALEVE dosage: TOTAL DAILY DOSE: 880 MG UNIT DOSE: 220 MG. During the same period patient was treated with MIRCADIS, HYDROCHLOROTHIAZIDE, GLYBURIDE, ATENOLOL. Patient recovered.
Humira Side Effects Report #5668635-6
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 26, 2008. Male patient, 32 years of age, was diagnosed with crohn's disease and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: fluid retention, injection site oedema, injection site reaction, oedema peripheral, skin disorder, . HUMIRA dosage: unknown. Patient recovered.
Tamiflu Side Effects Report #5669894-6
Physician from UNITED STATES reported TAMIFLU problem on Mar 14, 2008. Female patient, 44 years of age, weighting 172.0 lb, was diagnosed with influenza and was treated with TAMIFLU. After drug was administered, patient experienced the following problems/side effects: fluid retention, glossodynia, hypoaesthesia, sensation of heaviness, . TAMIFLU dosage: 75 MG BID PO. During the same period patient was treated with PHENERGAN, CODEINE COUGH MED. Patient recovered.
Lantus Side Effects Report #5672202-8
LANTUS problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Mar 12, 2008. Male patient was treated with LANTUS. After drug was administered, patient experienced the following problems/side effects: fluid retention, pneumonia, . LANTUS dosage: unknown. During the same period patient was treated with DIURETICS, NOVORAPID. Patient recovered.
Actos Side Effects Report #5688115-1
Consumer or non-health professional from UNITED STATES reported ACTOS problem on Mar 17, 2008. Male patient, 59 years of age, weighting 300.0 lb, was diagnosed with type 2 diabetes mellitus and was treated with ACTOS. After drug was administered, patient experienced the following problems/side effects: fluid retention, weight increased, . ACTOS dosage: 22.5 MG, 1 IN 1 D, PER ORAL. During the same period patient was treated with JANUVIA. Patient recovered.
Revlimid Side Effects Report #5689342-X
REVLIMID problem was reported by a Pharmacist from UNITED STATES on Mar 19, 2008. Female patient, 56 years of age, was diagnosed with amyloidosis and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: fluid retention, thrombocytopenia, weight increased, . REVLIMID dosage: 15 MG, DAILY 21/28 DAYS, ORAL; 10 MG, DAILY X21 DAYS, ORAL. During the same period patient was treated with DEXAMETHASONE, PREDNISONE. Patient was hospitalized. Patient recovered.
Starlix Side Effects Report #5611245-7
Consumer or non-health professional from UNITED STATES reported STARLIX problem on Jan 24, 2008. Female patient was treated with STARLIX. After drug was administered, patient experienced the following problems/side effects: fluid retention, renal impairment, weight increased, . STARLIX dosage: unknown. During the same period patient was treated with METFORMIN. Patient recovered.
Lyrica Side Effects Report #5613099-1
LYRICA problem was reported by a Physician from PORTUGAL on Jan 23, 2008. Female patient, 52 years of age, was diagnosed with neuralgia and was treated with LYRICA. After drug was administered, patient experienced the following problems/side effects: fluid retention, hypoxia, metabolic acidosis, oliguria, vomiting, . LYRICA dosage: unknown. During the same period patient was treated with ASPIRIN, PARACETAMOL, ANTIINFLAMMATORY. Patient was hospitalized. Patient recovered.
Lyrica Side Effects Report #5626795-7
Physician from FRANCE reported LYRICA problem on Feb 05, 2008. Male patient, 60 years of age, was diagnosed with diabetic neuropathy and was treated with LYRICA. After drug was administered, patient experienced the following problems/side effects: fluid retention, respiratory distress, sciatica, sodium retention, . LYRICA dosage: unknown. Patient recovered.
Januvia Side Effects Report #5627878-8
JANUVIA problem was reported by a Health Professional from UNITED STATES on Feb 11, 2008. Male patient, 60 years of age, was diagnosed with type 2 diabetes mellitus and was treated with JANUVIA. After drug was administered, patient experienced the following problems/side effects: fluid retention, . JANUVIA dosage: unknown. Patient was hospitalized. Patient recovered.
Divalproex Side Effects Report #5636761-3
Consumer or non-health professional from UNITED STATES reported DIVALPROEX problem on Feb 19, 2008. Male patient, 46 years of age, was treated with DIVALPROEX. After drug was administered, patient experienced the following problems/side effects: fluid retention, . DIVALPROEX dosage: 1500MG PM PO. Patient recovered.
Mirapex Side Effects Report #5639274-8
MIRAPEX problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 30, 2008. Male patient, 80 years of age, was diagnosed with restless legs syndrome, hypertension and was treated with MIRAPEX. After drug was administered, patient experienced the following problems/side effects: fluid retention, insomnia, . MIRAPEX dosage: unknown. During the same period patient was treated with NORVASC, DIOVAN, TOPROL. Patient recovered.
Januvia Side Effects Report #5655018-8
Physician from UNITED STATES reported JANUVIA problem on Nov 15, 2007. Male patient was diagnosed with type 2 diabetes mellitus and was treated with JANUVIA. After drug was administered, patient experienced the following problems/side effects: fluid retention, . JANUVIA dosage: unknown. Patient recovered.
Januvia Side Effects Report #5655145-5
JANUVIA problem was reported by a Physician from UNITED STATES on Oct 24, 2007. Female patient was treated with JANUVIA. After drug was administered, patient experienced the following problems/side effects: fluid retention, . JANUVIA dosage: unknown. Patient recovered.
Januvia Side Effects Report #5656893-3
Physician from UNITED STATES reported JANUVIA problem on Oct 22, 2007. Female patient was treated with JANUVIA. After drug was administered, patient experienced the following problems/side effects: fluid retention, oedema, . JANUVIA dosage: unknown. Patient recovered.
Januvia Side Effects Report #5657600-0
JANUVIA problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 26, 2007. Male patient, 72 years of age, was diagnosed with type 2 diabetes mellitus and was treated with JANUVIA. After drug was administered, patient experienced the following problems/side effects: fluid retention, . JANUVIA dosage: 100 MG/DAILY/PO. During the same period patient was treated with ACTONEL, ACTOS, CLINORIL, LIPITOR, NEXIUM, PLAVIX, PROSCAR, SYNTHROID. Patient recovered.
Letairis Side Effects Report #5587601-2
Pharmacist from UNITED STATES reported LETAIRIS problem on Jan 02, 2008. Female patient, weighting 160.1 lb, was diagnosed with pulmonary hypertension and was treated with LETAIRIS. After drug was administered, patient experienced the following problems/side effects: fluid retention, full blood count decreased, pneumonia, . LETAIRIS dosage: unknown. Patient was hospitalized. Patient recovered.
Rosiglitazone Side Effects Report #5588792-X
ROSIGLITAZONE problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Jan 11, 2008. Male patient, 68 years of age, weighting 198.4 lb, was treated with ROSIGLITAZONE. After drug was administered, patient experienced the following problems/side effects: fluid retention, oedema peripheral, pulmonary hypertension, pulmonary oedema, renal failure, . ROSIGLITAZONE dosage: unknown. During the same period patient was treated with SIMVASTATIN, TELMISARTAN, GLICLAZIDE, METFORMIN, VERAPAMIL, FUROSEMIDE. Patient was hospitalized. Patient recovered.
Letairis Side Effects Report #5600207-1
Pharmacist from UNITED STATES reported LETAIRIS problem on Jan 17, 2008. Female patient was diagnosed with pulmonary hypertension and was treated with LETAIRIS. After drug was administered, patient experienced the following problems/side effects: fluid retention, . LETAIRIS dosage: 5MG QD PO. Patient recovered.
Rosiglitazone Side Effects Report #5601299-6
ROSIGLITAZONE problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Jan 23, 2008. Male patient, 68 years of age, weighting 198.4 lb, was treated with ROSIGLITAZONE. After drug was administered, patient experienced the following problems/side effects: fluid retention, oedema peripheral, pulmonary hypertension, pulmonary oedema, renal failure, . ROSIGLITAZONE dosage: unknown. During the same period patient was treated with SIMVASTATIN, TELMISARTAN, GLICLAZIDE, METFORMIN, VERAPAMIL, FUROSEMIDE. Patient was hospitalized. Patient recovered.
Angeliq Side Effects Report #5603719-X
Consumer or non-health professional from UNITED STATES reported ANGELIQ problem on Oct 03, 2007. Female patient, 55 years of age, weighting 158.7 lb, was diagnosed with hypertension and was treated with ANGELIQ. After drug was administered, patient experienced the following problems/side effects: fluid retention, hot flush, insomnia, nervousness, weight increased, . ANGELIQ dosage: unknown. During the same period patient was treated with TRIAMTERENE AND HYDROCHLOROTHIAZID, ATENOLOL. Patient recovered.
Revlimid Side Effects Report #5628479-8
REVLIMID problem was reported by a Health Professional from UNITED STATES on Oct 26, 2007. Female patient was diagnosed with multiple myeloma and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: fluid retention, insomnia, nasopharyngitis, neuropathy peripheral, red blood cell count decreased, white blood cell count decreased, . REVLIMID dosage: 25 MG, QD, ORAL. During the same period patient was treated with LASIX, SLEEP AID. Patient recovered.
Revlimid Side Effects Report #5631235-8
Health Professional from UNITED STATES reported REVLIMID problem on Oct 26, 2007. Female patient, 68 years of age, was diagnosed with myelodysplastic syndrome and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: fluid retention, neutropenia, oedema peripheral, . REVLIMID dosage: 10 MG, 1 IN 1 D, ORAL. Patient recovered.
Revlimid Side Effects Report #5642046-1
REVLIMID problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 26, 2007. Male patient, 53 years of age, was diagnosed with multiple myeloma and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: fluid retention, rash, renal disorder, swelling, . REVLIMID dosage: 200 MG, 1 IN 1 D, ORAL. Patient recovered.
Byetta Side Effects Report #5652801-X
Consumer or non-health professional from UNITED STATES reported BYETTA problem on Oct 03, 2007. Male patient, 64 years of age, weighting 250.0 lb, was diagnosed with type 2 diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: fluid retention, headache, injection site haemorrhage, injection site pain, nausea, oedema peripheral, weight decreased, . BYETTA dosage: unknown. During the same period patient was treated with METFORMIN, ACTOS. Patient recovered.
Velcade Side Effects Report #5551276-9
VELCADE problem was reported by a Health Professional from ISRAEL on Nov 29, 2007. Female patient, 75 years of age, was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: fluid retention, hyponatraemia, thrombocytopenia, . VELCADE dosage: unknown. Patient was hospitalized. Patient recovered.
Fabrazyme Side Effects Report #5565353-X
Pharmacist from UNITED STATES reported FABRAZYME problem on Dec 10, 2007. Female patient, 58 years of age, weighting 220.0 lb, was diagnosed with fabry's disease and was treated with FABRAZYME. After drug was administered, patient experienced the following problems/side effects: fluid retention, non-small cell lung cancer, oedema peripheral, pain in extremity, swelling face, weight increased, . FABRAZYME dosage: 1 MG/KG Q2WKS IV. During the same period patient was treated with LASIX, STEROIDS. Patient recovered.
Detrusitol Side Effects Report #5570079-2
DETRUSITOL problem was reported by a Consumer or non-health professional from ARGENTINA on Dec 10, 2007. Female patient, weighting 187.4 lb, was diagnosed with urinary incontinence and was treated with DETRUSITOL. After drug was administered, patient experienced the following problems/side effects: fluid retention, oedema peripheral, . DETRUSITOL dosage: unknown. During the same period patient was treated with RISPERIDONE, VALSARTAN, DIUREX, ATENOLOL, VENLAFAXINE, LEVOTHYROXINE. Patient recovered.
Sprycel Side Effects Report #5571628-0
Consumer or non-health professional from UNITED STATES reported SPRYCEL problem on Nov 02, 2007. Male patient, 66 years of age, was diagnosed with chronic myeloid leukaemia and was treated with SPRYCEL. After drug was administered, patient experienced the following problems/side effects: fluid retention, pulmonary oedema, . SPRYCEL dosage: unknown. Patient recovered.
Estradiol Side Effects Report #5574331-6
ESTRADIOL problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 13, 2007. Female patient was diagnosed with parathyroid tumour and was treated with ESTRADIOL. After drug was administered, patient experienced the following problems/side effects: fluid retention, swelling, . ESTRADIOL dosage: unknown. During the same period patient was treated with PROVERA. Patient was hospitalized. Patient recovered.
Amlodipine Side Effects Report #5574698-9
Consumer or non-health professional from UNITED STATES reported AMLODIPINE problem on Dec 21, 2007. Female patient, weighting 150.0 lb, was diagnosed with hypertension and was treated with AMLODIPINE. After drug was administered, patient experienced the following problems/side effects: fluid retention, gait disturbance, . AMLODIPINE dosage: unknown. Patient recovered.
Campral Side Effects Report #5575661-4
CAMPRAL problem was reported by a Health Professional from FRANCE on Dec 10, 2007. Female patient was treated with CAMPRAL. After drug was administered, patient experienced the following problems/side effects: fluid retention, . CAMPRAL dosage: 333 MG QD PO. During the same period patient was treated with ANTIDEPRESSOR. Patient recovered.
Herceptin Side Effects Report #5576645-2
Physician from UNITED KINGDOM reported HERCEPTIN problem on Nov 18, 2007. Female patient, 35 years of age, was diagnosed with breast cancer metastatic and was treated with HERCEPTIN. After drug was administered, patient experienced the following problems/side effects: fluid retention, oedema, . HERCEPTIN dosage: 6 MG/KG, Q3W. During the same period patient was treated with TAXOTERE. Patient recovered.
Myfortic Side Effects Report #5503666-8
MYFORTIC problem was reported by a Physician from GREECE on Oct 24, 2007. Female patient was diagnosed with liver transplant and was treated with MYFORTIC. After drug was administered, patient experienced the following problems/side effects: fluid retention, ileus paralytic, . MYFORTIC dosage: 1440 MG/D. During the same period patient was treated with CERTICAN, MEDROL, FUNGOSTAL, AUGMENTIN, FLAGYL, VALSADE, SEPTRIN, ZURCAZOL. Patient recovered.
Prograf Side Effects Report #5510847-6
Health Professional from UNITED STATES reported PROGRAF problem on Oct 24, 2007. Male patient, 63 years of age, was diagnosed with renal transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: fluid retention, retroperitoneal effusion, . PROGRAF dosage: 2 MG, BID, ORAL. During the same period patient was treated with MYCOPHENOLATE MOFETIL, PREDNISONE, FUROSEMIDE, CLONIDINE, OMEPRAZOLE, ROSIGLITAZONE, VALGANCICLOVIR, BACTRIM DS. Patient was hospitalized. Patient recovered.
Avandamet Side Effects Report #5512419-6
AVANDAMET problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 20, 2006. Male patient, 59 years of age, weighting 175.3 lb, was treated with AVANDAMET. After drug was administered, patient experienced the following problems/side effects: fluid retention, oedema, weight increased, . AVANDAMET dosage: unknown. During the same period patient was treated with BENICAR, STATINS, LIPITOR. Patient recovered.
Avandamet Side Effects Report #5512460-3
Consumer or non-health professional from UNITED STATES reported AVANDAMET problem on Apr 20, 2007. Male patient, 51 years of age, was treated with AVANDAMET. After drug was administered, patient experienced the following problems/side effects: fluid retention, gait disturbance, joint swelling, weight increased, . AVANDAMET dosage: unknown. During the same period patient was treated with METOPROLOL TARTRATE, GLYCLAZIDE, LISINOPRIL, VYTORIN, PLAVIX, ASPIRIN. Patient recovered.
Avandamet Side Effects Report #5512527-X
AVANDAMET problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 20, 2007. Female patient, 54 years of age, weighting 174.4 lb, was treated with AVANDAMET. After drug was administered, patient experienced the following problems/side effects: fluid retention, oedema, weight increased, . AVANDAMET dosage: unknown. During the same period patient was treated with TARKA, DIOVAN, VYTORIN, LAMISIL, ASPIRIN. Patient recovered.
Coreg Side Effects Report #5515555-3
Consumer or non-health professional from UNITED STATES reported COREG problem on Apr 03, 2007. Female patient was diagnosed with hypertension and was treated with COREG. After drug was administered, patient experienced the following problems/side effects: fluid retention, oedema peripheral, swelling, weight increased, . COREG dosage: 12.5MG TWICE PER DAY. Patient recovered.
Commit Side Effects Report #5516529-9
COMMIT problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 13, 2007. Female patient, 61 years of age, was treated with COMMIT. After drug was administered, patient experienced the following problems/side effects: fluid retention, weight increased, . COMMIT dosage: unknown. Patient recovered.
Champix Side Effects Report #5518489-3
Physician from PORTUGAL reported CHAMPIX problem on Nov 07, 2007. Female patient, weighting 134.5 lb, was treated with CHAMPIX. After drug was administered, patient experienced the following problems/side effects: fluid retention, oedema peripheral, polyuria, urine output decreased, weight increased, . CHAMPIX dosage: unknown. Patient recovered.
Actos Side Effects Report #5520419-5
ACTOS problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 05, 2007. Female patient, 75 years of age, weighting 170.0 lb, was diagnosed with type 2 diabetes mellitus and was treated with ACTOS. After drug was administered, patient experienced the following problems/side effects: fluid retention, stress fracture, weight increased, . ACTOS dosage: 45 MG, QPM, PER ORAL. During the same period patient was treated with HYDROCHLOROTHIAZIDE, ALTACE, LIPITOR, DETROL. Patient recovered.
Betaseron Side Effects Report #5523927-6
Consumer or non-health professional from UNITED STATES reported BETASERON problem on Nov 20, 2007. Male patient, 40 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 retention, multiple sclerosis relapse, renal failure, . BETASERON dosage: unknown. Patient was hospitalized. Patient recovered.
Zyprexa Side Effects Report #5527882-4
ZYPREXA problem was reported by a Health Professional from UNITED STATES on Nov 26, 2007. Female patient, 58 years of age, weighting 140.0 lb, was diagnosed with major depression and was treated with ZYPREXA. After drug was administered, patient experienced the following problems/side effects: fluid retention, inflammation of wound, oedema peripheral, open wound, pitting oedema, weight increased, wound infection, wound secretion, . ZYPREXA dosage: 5 MG TWICE A DAY PO. Patient recovered.
Januvia Side Effects Report #5532823-X
Consumer or non-health professional from UNITED STATES reported JANUVIA problem on Sept 27, 2007. Female patient, 59 years of age, was diagnosed with type 2 diabetes mellitus and was treated with JANUVIA. After drug was administered, patient experienced the following problems/side effects: fluid retention, overdose, . JANUVIA dosage: 100 MG/BID/PO. During the same period patient was treated with INSULIN. Patient recovered.