Please choose an event type to view the corresponding MedsFacts report:

HEADACHE ( 23 FDA reports)
PYREXIA ( 21 FDA reports)
CHEST PAIN ( 18 FDA reports)
DIZZINESS ( 18 FDA reports)
NAUSEA ( 17 FDA reports)
ABDOMINAL PAIN ( 16 FDA reports)
ABSCESS ( 15 FDA reports)
BLOOD ALBUMIN DECREASED ( 14 FDA reports)
PAIN ( 14 FDA reports)
ANXIETY ( 13 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 13 FDA reports)
INFLAMMATION ( 13 FDA reports)
LYMPHADENOPATHY ( 13 FDA reports)
MUSCULOSKELETAL PAIN ( 13 FDA reports)
PNEUMONIA ( 13 FDA reports)
SWELLING ( 13 FDA reports)
VISUAL IMPAIRMENT ( 13 FDA reports)
VOMITING ( 13 FDA reports)
ALKALOSIS ( 12 FDA reports)
APLASTIC ANAEMIA ( 12 FDA reports)
ATELECTASIS ( 12 FDA reports)
BLINDNESS ( 12 FDA reports)
BLOOD CALCIUM DECREASED ( 12 FDA reports)
BLOOD POTASSIUM INCREASED ( 12 FDA reports)
CARBON DIOXIDE INCREASED ( 12 FDA reports)
CONSTIPATION ( 12 FDA reports)
DECREASED INTEREST ( 12 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 12 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 12 FDA reports)
GALLBLADDER DISORDER ( 12 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 12 FDA reports)
GRANULOMA ( 12 FDA reports)
HYDROCEPHALUS ( 12 FDA reports)
HYPERTENSION ( 12 FDA reports)
HYPOKALAEMIA ( 12 FDA reports)
MUCOSAL INFLAMMATION ( 12 FDA reports)
MULTIPLE SCLEROSIS ( 12 FDA reports)
OPTIC NEURITIS ( 12 FDA reports)
OSTEOARTHRITIS ( 12 FDA reports)
OSTEOMYELITIS ( 12 FDA reports)
OSTEONECROSIS OF JAW ( 12 FDA reports)
PARANASAL SINUS BENIGN NEOPLASM ( 12 FDA reports)
PATHOLOGICAL FRACTURE ( 12 FDA reports)
PLEURAL EFFUSION ( 12 FDA reports)
PULMONARY ARTERY DILATATION ( 12 FDA reports)
PULMONARY OEDEMA ( 12 FDA reports)
RENAL DISORDER ( 12 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 12 FDA reports)
SARCOIDOSIS ( 12 FDA reports)
TUBERCULOSIS ( 12 FDA reports)
UTERINE LEIOMYOMA ( 12 FDA reports)
CSF PROTEIN INCREASED ( 11 FDA reports)
DYSPNOEA ( 11 FDA reports)
NASAL DISORDER ( 11 FDA reports)
RIB FRACTURE ( 11 FDA reports)
FATIGUE ( 10 FDA reports)
ARTHRALGIA ( 9 FDA reports)
BONE DEBRIDEMENT ( 9 FDA reports)
HYSTERECTOMY ( 9 FDA reports)
JOINT SURGERY ( 9 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ( 9 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 9 FDA reports)
TOOTH EXTRACTION ( 9 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 9 FDA reports)
VENTRICULO-PERITONEAL SHUNT ( 9 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 7 FDA reports)
HYPOAESTHESIA ( 7 FDA reports)
MONOCYTE COUNT INCREASED ( 7 FDA reports)
NEPHROSCLEROSIS ( 7 FDA reports)
RENAL FAILURE CHRONIC ( 7 FDA reports)
SEPSIS ( 7 FDA reports)
SINUS RHYTHM ( 7 FDA reports)
ALVEOLOPLASTY ( 6 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 6 FDA reports)
DRUG INEFFECTIVE ( 6 FDA reports)
INFUSION RELATED REACTION ( 6 FDA reports)
PALPITATIONS ( 6 FDA reports)
PANCREATITIS ( 6 FDA reports)
PEAU D'ORANGE ( 6 FDA reports)
POLLAKIURIA ( 6 FDA reports)
RADIATION SKIN INJURY ( 6 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 6 FDA reports)
WEIGHT INCREASED ( 6 FDA reports)
BONE LESION ( 5 FDA reports)
DEHYDRATION ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
GAIT DISTURBANCE ( 5 FDA reports)
HAEMATOCHEZIA ( 5 FDA reports)
INTESTINAL POLYP ( 5 FDA reports)
MEMORY IMPAIRMENT ( 5 FDA reports)
MENTAL STATUS CHANGES ( 5 FDA reports)
NASAL SEPTUM DEVIATION ( 5 FDA reports)
PARAESTHESIA ( 5 FDA reports)
SINUS POLYP ( 5 FDA reports)
SYNCOPE ( 5 FDA reports)
WALKING AID USER ( 5 FDA reports)
CERVICITIS ( 4 FDA reports)
CHEST DISCOMFORT ( 4 FDA reports)
CROHN'S DISEASE ( 4 FDA reports)
INFLUENZA LIKE ILLNESS ( 4 FDA reports)
JOINT SWELLING ( 4 FDA reports)
METAPLASIA ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
OVARIAN ATROPHY ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
CHILLS ( 3 FDA reports)
COLONIC POLYP ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
COUGH ( 3 FDA reports)
DEATH ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
GASTRIC POLYPS ( 3 FDA reports)
GASTRITIS ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
MELANOSIS COLI ( 3 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
NOCTURIA ( 3 FDA reports)
PLEURITIC PAIN ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
RENAL TUBULAR NECROSIS ( 3 FDA reports)
TREMOR ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
ALOPECIA ( 2 FDA reports)
APHONIA ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BONE DISORDER ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
COLECTOMY ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
ENTEROCUTANEOUS FISTULA ( 2 FDA reports)
EXPIRED DRUG ADMINISTERED ( 2 FDA reports)
FALL ( 2 FDA reports)
FISTULA DISCHARGE ( 2 FDA reports)
GASTRIC NEOPLASM ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HIP FRACTURE ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
INFUSION SITE REACTION ( 2 FDA reports)
INJECTION SITE PRURITUS ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 2 FDA reports)
JOINT STIFFNESS ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MENINGITIS ASEPTIC ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
MUSCLE SPASTICITY ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
NEPHRITIS INTERSTITIAL ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
OROPHARYNGEAL SWELLING ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
ULCER ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ACCIDENTAL NEEDLE STICK ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYST ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GLIOSIS ( 1 FDA reports)
GLOMERULOSCLEROSIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INCISION SITE INFECTION ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INGUINAL HERNIA ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INTESTINAL STENOSIS ( 1 FDA reports)
KERATITIS ( 1 FDA reports)
KIDNEY FIBROSIS ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LENTICULAR OPACITIES ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
LYMPHOHISTIOCYTOSIS ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MENIERE'S DISEASE ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEOPLASM SKIN ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHARYNGEAL ERYTHEMA ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
RENAL ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL TUBULAR ATROPHY ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SCAR ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SNORING ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SUBCUTANEOUS ABSCESS ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
TONSILLAR HYPERTROPHY ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use