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

CROHN'S DISEASE ( 29 FDA reports)
DIARRHOEA ( 29 FDA reports)
ARTHRALGIA ( 25 FDA reports)
CHEST PAIN ( 21 FDA reports)
FATIGUE ( 21 FDA reports)
ABDOMINAL PAIN ( 20 FDA reports)
ASTHENIA ( 20 FDA reports)
PRURITUS ( 20 FDA reports)
PYREXIA ( 20 FDA reports)
DRUG INEFFECTIVE ( 18 FDA reports)
INJECTION SITE PAIN ( 18 FDA reports)
NAUSEA ( 18 FDA reports)
RASH ( 17 FDA reports)
OROPHARYNGEAL PAIN ( 16 FDA reports)
COLITIS ( 15 FDA reports)
COUGH ( 15 FDA reports)
JOINT SWELLING ( 15 FDA reports)
DRUG INTERACTION ( 14 FDA reports)
INFLUENZA ( 14 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 14 FDA reports)
WEIGHT DECREASED ( 14 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 13 FDA reports)
LYMPHADENOPATHY ( 13 FDA reports)
NASAL CONGESTION ( 13 FDA reports)
INFLAMMATION ( 12 FDA reports)
NASOPHARYNGITIS ( 12 FDA reports)
PAIN ( 12 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 12 FDA reports)
DYSPNOEA ( 11 FDA reports)
INFUSION RELATED REACTION ( 11 FDA reports)
NEPHRITIS ( 11 FDA reports)
OEDEMA MOUTH ( 11 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 11 FDA reports)
SKIN DISCOLOURATION ( 11 FDA reports)
INJECTION SITE ERYTHEMA ( 10 FDA reports)
MYOCARDIAL INFARCTION ( 10 FDA reports)
SCRATCH ( 10 FDA reports)
VOMITING ( 10 FDA reports)
WOUND HAEMORRHAGE ( 10 FDA reports)
ADVERSE DRUG REACTION ( 9 FDA reports)
DRUG DOSE OMISSION ( 9 FDA reports)
GINGIVAL SWELLING ( 9 FDA reports)
HEADACHE ( 9 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 9 FDA reports)
COLITIS ULCERATIVE ( 8 FDA reports)
INFECTION ( 8 FDA reports)
INJECTION SITE PRURITUS ( 8 FDA reports)
INTESTINAL STENOSIS ( 8 FDA reports)
URINARY TRACT INFLAMMATION ( 8 FDA reports)
ANASTOMOTIC COMPLICATION ( 7 FDA reports)
FISTULA ( 7 FDA reports)
MALAISE ( 7 FDA reports)
OEDEMA PERIPHERAL ( 7 FDA reports)
STOMATITIS ( 7 FDA reports)
WEIGHT INCREASED ( 7 FDA reports)
ABDOMINAL PAIN UPPER ( 6 FDA reports)
DEHYDRATION ( 6 FDA reports)
ERYTHEMA ( 6 FDA reports)
HAEMATOCHEZIA ( 6 FDA reports)
INJECTION SITE HAEMATOMA ( 6 FDA reports)
MYALGIA ( 6 FDA reports)
NECK PAIN ( 6 FDA reports)
RECTAL HAEMORRHAGE ( 6 FDA reports)
UNEVALUABLE EVENT ( 6 FDA reports)
ABSCESS ( 5 FDA reports)
ANAEMIA ( 5 FDA reports)
ARTHRITIS ( 5 FDA reports)
ARTHROPATHY ( 5 FDA reports)
BASAL CELL CARCINOMA ( 5 FDA reports)
BLOOD PRESSURE INCREASED ( 5 FDA reports)
CHONDROPATHY ( 5 FDA reports)
MUSCLE SPASMS ( 5 FDA reports)
OFF LABEL USE ( 5 FDA reports)
PAIN IN EXTREMITY ( 5 FDA reports)
ABDOMINAL DISCOMFORT ( 4 FDA reports)
CHILLS ( 4 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
EYE SWELLING ( 4 FDA reports)
HAEMORRHAGE ( 4 FDA reports)
HERPES ZOSTER ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
INJECTION SITE HAEMORRHAGE ( 4 FDA reports)
INJECTION SITE REACTION ( 4 FDA reports)
INJECTION SITE SWELLING ( 4 FDA reports)
INJECTION SITE WARMTH ( 4 FDA reports)
LIP SWELLING ( 4 FDA reports)
NEPHROLITHIASIS ( 4 FDA reports)
SINUSITIS ( 4 FDA reports)
SWELLING FACE ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 4 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 3 FDA reports)
ABSCESS LIMB ( 3 FDA reports)
ACNE ( 3 FDA reports)
ANORECTAL DISORDER ( 3 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 3 FDA reports)
BRONCHITIS ( 3 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 3 FDA reports)
DEVICE MALFUNCTION ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
FALL ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HOT FLUSH ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
IRON DEFICIENCY ANAEMIA ( 3 FDA reports)
JOINT STIFFNESS ( 3 FDA reports)
METASTASES TO LIVER ( 3 FDA reports)
MIGRAINE ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
PANCREATITIS ( 3 FDA reports)
POLYP ( 3 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 3 FDA reports)
SKELETAL INJURY ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
URINARY TRACT OBSTRUCTION ( 3 FDA reports)
VIRAL INFECTION ( 3 FDA reports)
ALOPECIA ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
BACK DISORDER ( 2 FDA reports)
BILIARY COLIC ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CHOLECYSTITIS ACUTE ( 2 FDA reports)
CLEFT LIP AND PALATE ( 2 FDA reports)
COLONIC OBSTRUCTION ( 2 FDA reports)
COLONIC POLYP ( 2 FDA reports)
COLONIC STENOSIS ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
DEFAECATION URGENCY ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
EATING DISORDER ( 2 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 2 FDA reports)
ERYTHEMA NODOSUM ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
EYE PRURITUS ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 2 FDA reports)
GASTROINTESTINAL PAIN ( 2 FDA reports)
HEPATOSPLENOMEGALY ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPERSOMNIA ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
INFUSION SITE ERYTHEMA ( 2 FDA reports)
INJECTION SITE INDURATION ( 2 FDA reports)
INJECTION SITE NODULE ( 2 FDA reports)
INJECTION SITE URTICARIA ( 2 FDA reports)
JOINT LOCK ( 2 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 2 FDA reports)
LARYNGEAL CANCER ( 2 FDA reports)
LOCAL SWELLING ( 2 FDA reports)
LUNG CANCER METASTATIC ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
MUSCLE DISORDER ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
NASAL OEDEMA ( 2 FDA reports)
NECK MASS ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OESOPHAGEAL SPASM ( 2 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 2 FDA reports)
PALMAR ERYTHEMA ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PERICARDITIS ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RASH VESICULAR ( 2 FDA reports)
RECTAL ABSCESS ( 2 FDA reports)
RECTAL FISSURE ( 2 FDA reports)
RHINALGIA ( 2 FDA reports)
SCAB ( 2 FDA reports)
SECRETION DISCHARGE ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
SUBCUTANEOUS ABSCESS ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
CONCUSSION ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CRYPTOSPORIDIOSIS INFECTION ( 1 FDA reports)
DEATH ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DISSEMINATED LARGE CELL LYMPHOMA ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG TOLERANCE ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
ILEITIS ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INCISION SITE INFECTION ( 1 FDA reports)
INCISIONAL DRAINAGE ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCORRECT PRODUCT STORAGE ( 1 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INFUSION SITE CELLULITIS ( 1 FDA reports)
INJECTION SITE ANAESTHESIA ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE OEDEMA ( 1 FDA reports)
INJECTION SITE PAPULE ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
INTESTINAL RESECTION ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JEJUNAL ULCER ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MENSTRUAL DISORDER ( 1 FDA reports)
MENSTRUATION DELAYED ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PERIRECTAL ABSCESS ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RECTAL OBSTRUCTION ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RETROGRADE AMNESIA ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SERONEGATIVE ARTHRITIS ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SMALL INTESTINE ULCER ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
SYNOVIAL CYST ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
THROMBOCYTOSIS ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TRAUMATIC LUNG INJURY ( 1 FDA reports)
TREMOR ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VITAMIN A DECREASED ( 1 FDA reports)
VITAMIN C DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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