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

GASTROINTESTINAL DISORDER ( 2246 FDA reports)
DRUG INEFFECTIVE ( 2068 FDA reports)
RECTAL DISCHARGE ( 1959 FDA reports)
WEIGHT INCREASED ( 1775 FDA reports)
CONSTIPATION ( 1709 FDA reports)
FLATULENCE ( 1493 FDA reports)
DIARRHOEA ( 1255 FDA reports)
ABDOMINAL PAIN UPPER ( 1118 FDA reports)
HEADACHE ( 964 FDA reports)
ABDOMINAL DISTENSION ( 959 FDA reports)
STEATORRHOEA ( 889 FDA reports)
MALAISE ( 811 FDA reports)
NAUSEA ( 790 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 687 FDA reports)
FATIGUE ( 557 FDA reports)
ABDOMINAL PAIN ( 485 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 484 FDA reports)
DIZZINESS ( 483 FDA reports)
RECTAL HAEMORRHAGE ( 436 FDA reports)
MUSCLE SPASMS ( 430 FDA reports)
PAIN ( 417 FDA reports)
WEIGHT FLUCTUATION ( 397 FDA reports)
VOMITING ( 393 FDA reports)
HUNGER ( 370 FDA reports)
FAECES DISCOLOURED ( 351 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 347 FDA reports)
FEELING ABNORMAL ( 334 FDA reports)
FOOD CRAVING ( 323 FDA reports)
ANOREXIA ( 293 FDA reports)
ASTHENIA ( 290 FDA reports)
HAEMATOCHEZIA ( 275 FDA reports)
ILL-DEFINED DISORDER ( 275 FDA reports)
FAECAL INCONTINENCE ( 260 FDA reports)
BACK PAIN ( 250 FDA reports)
ADVERSE EVENT ( 232 FDA reports)
DEFAECATION URGENCY ( 225 FDA reports)
INSOMNIA ( 220 FDA reports)
DYSPNOEA ( 214 FDA reports)
MIGRAINE ( 199 FDA reports)
RASH ( 196 FDA reports)
STOMACH DISCOMFORT ( 195 FDA reports)
PAIN IN EXTREMITY ( 190 FDA reports)
ANXIETY ( 189 FDA reports)
HEPATIC ENZYME INCREASED ( 189 FDA reports)
GASTROENTERITIS VIRAL ( 186 FDA reports)
NASOPHARYNGITIS ( 186 FDA reports)
DEPRESSION ( 182 FDA reports)
HYPERPHAGIA ( 176 FDA reports)
FLUID RETENTION ( 166 FDA reports)
DYSPEPSIA ( 164 FDA reports)
STRESS ( 161 FDA reports)
PRURITUS ( 156 FDA reports)
MENSTRUAL DISORDER ( 151 FDA reports)
POLLAKIURIA ( 151 FDA reports)
ABNORMAL FAECES ( 149 FDA reports)
ARTHRALGIA ( 148 FDA reports)
OEDEMA PERIPHERAL ( 145 FDA reports)
INFLUENZA ( 144 FDA reports)
CHANGE OF BOWEL HABIT ( 141 FDA reports)
CHEST PAIN ( 141 FDA reports)
FRUSTRATION ( 140 FDA reports)
HYPERSENSITIVITY ( 135 FDA reports)
DISCOMFORT ( 134 FDA reports)
MENSTRUATION IRREGULAR ( 132 FDA reports)
URTICARIA ( 127 FDA reports)
COUGH ( 124 FDA reports)
PYREXIA ( 124 FDA reports)
NEPHROLITHIASIS ( 122 FDA reports)
MENSTRUATION DELAYED ( 115 FDA reports)
LOSS OF CONSCIOUSNESS ( 114 FDA reports)
DECREASED APPETITE ( 110 FDA reports)
ASTHMA ( 109 FDA reports)
FEAR ( 109 FDA reports)
CHOLELITHIASIS ( 105 FDA reports)
DEHYDRATION ( 102 FDA reports)
NONSPECIFIC REACTION ( 102 FDA reports)
THIRST ( 102 FDA reports)
ALOPECIA ( 98 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 97 FDA reports)
GASTRIC DISORDER ( 96 FDA reports)
ABDOMINAL DISCOMFORT ( 95 FDA reports)
ANAL HAEMORRHAGE ( 91 FDA reports)
DRUG INTERACTION ( 90 FDA reports)
SINUSITIS ( 89 FDA reports)
DEPRESSED MOOD ( 87 FDA reports)
GALLBLADDER DISORDER ( 86 FDA reports)
INCREASED APPETITE ( 86 FDA reports)
MYALGIA ( 86 FDA reports)
EATING DISORDER ( 85 FDA reports)
BLOOD PRESSURE INCREASED ( 83 FDA reports)
DYSGEUSIA ( 81 FDA reports)
HYPERHIDROSIS ( 79 FDA reports)
CHROMATURIA ( 78 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 78 FDA reports)
PALPITATIONS ( 77 FDA reports)
VAGINAL HAEMORRHAGE ( 77 FDA reports)
HYPERTENSION ( 72 FDA reports)
ABDOMINAL PAIN LOWER ( 71 FDA reports)
PREMENSTRUAL SYNDROME ( 71 FDA reports)
JOINT SWELLING ( 70 FDA reports)
NERVOUSNESS ( 69 FDA reports)
BRONCHITIS ( 68 FDA reports)
SOMNOLENCE ( 68 FDA reports)
PRODUCT QUALITY ISSUE ( 67 FDA reports)
GASTROINTESTINAL PAIN ( 66 FDA reports)
MENORRHAGIA ( 66 FDA reports)
POOR QUALITY SLEEP ( 66 FDA reports)
TREMOR ( 66 FDA reports)
INTENTIONAL DRUG MISUSE ( 64 FDA reports)
BACK DISORDER ( 63 FDA reports)
DRY MOUTH ( 63 FDA reports)
PANCREATITIS ( 63 FDA reports)
FALL ( 62 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 59 FDA reports)
DIVERTICULITIS ( 59 FDA reports)
SLUGGISHNESS ( 59 FDA reports)
PNEUMONIA ( 58 FDA reports)
GAIT DISTURBANCE ( 56 FDA reports)
METRORRHAGIA ( 55 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 54 FDA reports)
HAEMORRHOIDS ( 53 FDA reports)
HYPOAESTHESIA ( 53 FDA reports)
OBSESSIVE THOUGHTS ( 53 FDA reports)
SYNCOPE ( 53 FDA reports)
BINGE EATING ( 52 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 52 FDA reports)
PROCTALGIA ( 52 FDA reports)
TREATMENT NONCOMPLIANCE ( 52 FDA reports)
EMOTIONAL DISORDER ( 51 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 51 FDA reports)
ADVERSE DRUG REACTION ( 50 FDA reports)
ENERGY INCREASED ( 50 FDA reports)
ERYTHEMA ( 50 FDA reports)
HOT FLUSH ( 50 FDA reports)
IRRITABLE BOWEL SYNDROME ( 50 FDA reports)
NECK PAIN ( 50 FDA reports)
HEART RATE INCREASED ( 49 FDA reports)
FEELING COLD ( 48 FDA reports)
HAEMORRHAGE ( 48 FDA reports)
JOINT INJURY ( 48 FDA reports)
MYOCARDIAL INFARCTION ( 48 FDA reports)
SLEEP DISORDER ( 48 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 48 FDA reports)
ARTHROPATHY ( 47 FDA reports)
LIPIDURIA ( 47 FDA reports)
POLYMENORRHOEA ( 47 FDA reports)
SWELLING ( 47 FDA reports)
PRESYNCOPE ( 46 FDA reports)
BLOOD URINE PRESENT ( 43 FDA reports)
CHEST DISCOMFORT ( 42 FDA reports)
IRRITABILITY ( 42 FDA reports)
SALT CRAVING ( 42 FDA reports)
CHOLECYSTECTOMY ( 41 FDA reports)
FAECES HARD ( 41 FDA reports)
MUSCULOSKELETAL PAIN ( 41 FDA reports)
RENAL PAIN ( 41 FDA reports)
CONVULSION ( 40 FDA reports)
LIMB INJURY ( 40 FDA reports)
LIVER INJURY ( 40 FDA reports)
MOBILITY DECREASED ( 40 FDA reports)
MULTIPLE ALLERGIES ( 40 FDA reports)
WEIGHT DECREASED ( 40 FDA reports)
DYSMENORRHOEA ( 39 FDA reports)
URINARY TRACT INFECTION ( 39 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 38 FDA reports)
RASH PRURITIC ( 38 FDA reports)
SINUS HEADACHE ( 38 FDA reports)
BLOOD GLUCOSE DECREASED ( 37 FDA reports)
DRUG ADMINISTRATION ERROR ( 37 FDA reports)
ANAEMIA ( 36 FDA reports)
CONDITION AGGRAVATED ( 36 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 36 FDA reports)
INTESTINAL OBSTRUCTION ( 36 FDA reports)
PRURITUS GENERALISED ( 36 FDA reports)
BALANCE DISORDER ( 35 FDA reports)
FAECES PALE ( 35 FDA reports)
EMOTIONAL DISTRESS ( 34 FDA reports)
COLITIS ( 33 FDA reports)
SWELLING FACE ( 33 FDA reports)
BLOOD BILIRUBIN INCREASED ( 32 FDA reports)
DYSPHAGIA ( 32 FDA reports)
INITIAL INSOMNIA ( 32 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 32 FDA reports)
POLYDIPSIA ( 32 FDA reports)
VIRAL INFECTION ( 32 FDA reports)
ACNE ( 31 FDA reports)
CHILLS ( 31 FDA reports)
FAECAL VOLUME DECREASED ( 31 FDA reports)
FEELING HOT ( 31 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 31 FDA reports)
HYPOTENSION ( 31 FDA reports)
HYPOTHYROIDISM ( 31 FDA reports)
JOINT SPRAIN ( 31 FDA reports)
LUNG DISORDER ( 31 FDA reports)
MENTAL IMPAIRMENT ( 31 FDA reports)
RASH GENERALISED ( 31 FDA reports)
DISTURBANCE IN ATTENTION ( 30 FDA reports)
FEELING JITTERY ( 30 FDA reports)
FIBROMYALGIA ( 30 FDA reports)
HEPATIC STEATOSIS ( 30 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 30 FDA reports)
NERVE COMPRESSION ( 30 FDA reports)
ANORECTAL DISCOMFORT ( 29 FDA reports)
APPENDICITIS ( 29 FDA reports)
DRY SKIN ( 29 FDA reports)
OFF LABEL USE ( 29 FDA reports)
TENDERNESS ( 29 FDA reports)
THYROID DISORDER ( 29 FDA reports)
BLINDNESS ( 28 FDA reports)
DIABETES MELLITUS ( 28 FDA reports)
MUSCLE TIGHTNESS ( 28 FDA reports)
SKIN ODOUR ABNORMAL ( 28 FDA reports)
CELLULITIS ( 27 FDA reports)
CONFUSIONAL STATE ( 27 FDA reports)
EPISTAXIS ( 27 FDA reports)
HEPATITIS ( 27 FDA reports)
INFECTED CYST ( 27 FDA reports)
INFLUENZA LIKE ILLNESS ( 27 FDA reports)
SUBCUTANEOUS ABSCESS ( 27 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 26 FDA reports)
BURNING SENSATION ( 26 FDA reports)
CONTUSION ( 26 FDA reports)
EYE SWELLING ( 26 FDA reports)
INFECTION ( 26 FDA reports)
NERVE BLOCK ( 26 FDA reports)
SENSATION OF HEAVINESS ( 26 FDA reports)
URINE ODOUR ABNORMAL ( 26 FDA reports)
BACK INJURY ( 25 FDA reports)
ERUCTATION ( 25 FDA reports)
FOOD POISONING ( 25 FDA reports)
HORMONE LEVEL ABNORMAL ( 25 FDA reports)
LOCAL SWELLING ( 25 FDA reports)
SURGERY ( 25 FDA reports)
ARTHRITIS ( 24 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 24 FDA reports)
BLOOD POTASSIUM DECREASED ( 24 FDA reports)
CRYING ( 24 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 24 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 24 FDA reports)
EYE DISORDER ( 24 FDA reports)
EYE PAIN ( 24 FDA reports)
LETHARGY ( 24 FDA reports)
PANCREATITIS ACUTE ( 24 FDA reports)
BLOOD GLUCOSE INCREASED ( 23 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 23 FDA reports)
GASTROINTESTINAL INFECTION ( 23 FDA reports)
MOOD ALTERED ( 23 FDA reports)
NOCTURIA ( 23 FDA reports)
PAINFUL DEFAECATION ( 23 FDA reports)
SUNBURN ( 23 FDA reports)
THROMBOSIS ( 23 FDA reports)
VERTIGO ( 23 FDA reports)
BREAST CANCER ( 22 FDA reports)
CATARACT ( 22 FDA reports)
DYSURIA ( 22 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 22 FDA reports)
JAUNDICE ( 22 FDA reports)
RASH MACULAR ( 22 FDA reports)
RHINORRHOEA ( 22 FDA reports)
SEASONAL ALLERGY ( 22 FDA reports)
VAGINAL DISCHARGE ( 22 FDA reports)
ABASIA ( 21 FDA reports)
BLOOD PRESSURE DECREASED ( 21 FDA reports)
COAGULOPATHY ( 21 FDA reports)
HYPOMENORRHOEA ( 21 FDA reports)
KIDNEY INFECTION ( 21 FDA reports)
LAZINESS ( 21 FDA reports)
LIP PAIN ( 21 FDA reports)
OROPHARYNGEAL PAIN ( 21 FDA reports)
PARAESTHESIA ( 21 FDA reports)
SENSORY DISTURBANCE ( 21 FDA reports)
SINUS DISORDER ( 21 FDA reports)
SKIN LACERATION ( 21 FDA reports)
SWOLLEN TONGUE ( 21 FDA reports)
AMENORRHOEA ( 20 FDA reports)
ANKLE FRACTURE ( 20 FDA reports)
CYSTITIS ( 20 FDA reports)
EXOSTOSIS ( 20 FDA reports)
HAEMATEMESIS ( 20 FDA reports)
HEPATIC FAILURE ( 20 FDA reports)
LIMB DISCOMFORT ( 20 FDA reports)
LIVER DISORDER ( 20 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 20 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 20 FDA reports)
ORAL HERPES ( 20 FDA reports)
STAPHYLOCOCCAL INFECTION ( 20 FDA reports)
VISION BLURRED ( 20 FDA reports)
AMNESIA ( 19 FDA reports)
ATRIAL FIBRILLATION ( 19 FDA reports)
BLOOD IRON DECREASED ( 19 FDA reports)
BUNION ( 19 FDA reports)
HERPES ZOSTER ( 19 FDA reports)
INCISION SITE HAEMORRHAGE ( 19 FDA reports)
ACCIDENT ( 18 FDA reports)
BLISTER ( 18 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 18 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 18 FDA reports)
HAEMATURIA ( 18 FDA reports)
INGROWING NAIL ( 18 FDA reports)
MULTIPLE SCLEROSIS ( 18 FDA reports)
MUSCLE STRAIN ( 18 FDA reports)
OEDEMA ( 18 FDA reports)
SELF-INJURIOUS IDEATION ( 18 FDA reports)
THERMAL BURN ( 18 FDA reports)
THROAT TIGHTNESS ( 18 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 18 FDA reports)
CHOLECYSTITIS ( 17 FDA reports)
CIRCULATORY COLLAPSE ( 17 FDA reports)
COLITIS ULCERATIVE ( 17 FDA reports)
HIP FRACTURE ( 17 FDA reports)
LIP SWELLING ( 17 FDA reports)
OCULAR HYPERAEMIA ( 17 FDA reports)
OPTIC NEURITIS ( 17 FDA reports)
PHARYNGEAL OEDEMA ( 17 FDA reports)
PROCEDURAL PAIN ( 17 FDA reports)
RASH ERYTHEMATOUS ( 17 FDA reports)
ABORTION SPONTANEOUS ( 16 FDA reports)
DYSKINESIA ( 16 FDA reports)
FUNGAL INFECTION ( 16 FDA reports)
GASTRITIS ( 16 FDA reports)
HYPOGLYCAEMIA ( 16 FDA reports)
MEDICATION ERROR ( 16 FDA reports)
MENOPAUSAL SYMPTOMS ( 16 FDA reports)
MICTURITION URGENCY ( 16 FDA reports)
RETCHING ( 16 FDA reports)
TACHYCARDIA ( 16 FDA reports)
VISUAL DISTURBANCE ( 16 FDA reports)
YELLOW SKIN ( 16 FDA reports)
ABNORMAL BEHAVIOUR ( 15 FDA reports)
BENIGN NEOPLASM ( 15 FDA reports)
CARDIAC DISORDER ( 15 FDA reports)
COLD SWEAT ( 15 FDA reports)
DYSSTASIA ( 15 FDA reports)
MUSCULAR WEAKNESS ( 15 FDA reports)
OLIGODIPSIA ( 15 FDA reports)
PANIC ATTACK ( 15 FDA reports)
TRANSAMINASES INCREASED ( 15 FDA reports)
APATHY ( 14 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 14 FDA reports)
BREAST PAIN ( 14 FDA reports)
FEELINGS OF WORTHLESSNESS ( 14 FDA reports)
GASTRIC ULCER ( 14 FDA reports)
PULSE ABNORMAL ( 14 FDA reports)
SKIN DISCOLOURATION ( 14 FDA reports)
BLOOD TEST ABNORMAL ( 13 FDA reports)
COLONOSCOPY ( 13 FDA reports)
DEPENDENCE ( 13 FDA reports)
EXPIRED DRUG ADMINISTERED ( 13 FDA reports)
GROIN PAIN ( 13 FDA reports)
MEDIAL TIBIAL STRESS SYNDROME ( 13 FDA reports)
OVERDOSE ( 13 FDA reports)
WEIGHT LOSS POOR ( 13 FDA reports)
ABNORMAL DREAMS ( 12 FDA reports)
ANAL DISCOMFORT ( 12 FDA reports)
ANGINA PECTORIS ( 12 FDA reports)
FLUSHING ( 12 FDA reports)
HYPERTHYROIDISM ( 12 FDA reports)
INCISION SITE PAIN ( 12 FDA reports)
INFLAMMATION ( 12 FDA reports)
MUCOUS STOOLS ( 12 FDA reports)
RECTAL TENESMUS ( 12 FDA reports)
RENAL IMPAIRMENT ( 12 FDA reports)
SKIN ATROPHY ( 12 FDA reports)
ACUTE HEPATIC FAILURE ( 11 FDA reports)
ADVERSE REACTION ( 11 FDA reports)
AGGRESSION ( 11 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 11 FDA reports)
BREAST TENDERNESS ( 11 FDA reports)
CEREBROVASCULAR ACCIDENT ( 11 FDA reports)
COLON CANCER ( 11 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 11 FDA reports)
HYPERSOMNIA ( 11 FDA reports)
LACK OF SATIETY ( 11 FDA reports)
LIBIDO DECREASED ( 11 FDA reports)
MEMORY IMPAIRMENT ( 11 FDA reports)
MENTAL DISORDER ( 11 FDA reports)
MENTAL STATUS CHANGES ( 11 FDA reports)
MIDDLE INSOMNIA ( 11 FDA reports)
RHEUMATOID ARTHRITIS ( 11 FDA reports)
THYROID NEOPLASM ( 11 FDA reports)
TINNITUS ( 11 FDA reports)
TOOTHACHE ( 11 FDA reports)
URINE ABNORMALITY ( 11 FDA reports)
VISUAL IMPAIRMENT ( 11 FDA reports)
ANAPHYLACTIC SHOCK ( 10 FDA reports)
APPENDICECTOMY ( 10 FDA reports)
EPILEPSY ( 10 FDA reports)
EYELID OEDEMA ( 10 FDA reports)
FAECAL VOLUME INCREASED ( 10 FDA reports)
FOOT FRACTURE ( 10 FDA reports)
GALLBLADDER PAIN ( 10 FDA reports)
JOINT STIFFNESS ( 10 FDA reports)
LABORATORY TEST ABNORMAL ( 10 FDA reports)
LIPASE INCREASED ( 10 FDA reports)
LIVER TRANSPLANT ( 10 FDA reports)
NASAL CONGESTION ( 10 FDA reports)
PALLOR ( 10 FDA reports)
PANCREATIC ENZYMES INCREASED ( 10 FDA reports)
PHOTOSENSITIVITY REACTION ( 10 FDA reports)
RENAL FAILURE ACUTE ( 10 FDA reports)
STARVATION ( 10 FDA reports)
SUICIDAL IDEATION ( 10 FDA reports)
THYROIDITIS ( 10 FDA reports)
TYPE 2 DIABETES MELLITUS ( 10 FDA reports)
URINE OUTPUT DECREASED ( 10 FDA reports)
VISUAL ACUITY REDUCED ( 10 FDA reports)
APPETITE DISORDER ( 9 FDA reports)
BLOOD AMYLASE INCREASED ( 9 FDA reports)
BODY TEMPERATURE INCREASED ( 9 FDA reports)
BREATH ODOUR ( 9 FDA reports)
CARDIOVASCULAR DISORDER ( 9 FDA reports)
DRUG EFFECT DECREASED ( 9 FDA reports)
EAR INFECTION ( 9 FDA reports)
HAEMOGLOBIN DECREASED ( 9 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 9 FDA reports)
HEPATITIS ACUTE ( 9 FDA reports)
HEPATOMEGALY ( 9 FDA reports)
HYPERCHLORHYDRIA ( 9 FDA reports)
HYPOVITAMINOSIS ( 9 FDA reports)
IRON DEFICIENCY ANAEMIA ( 9 FDA reports)
JOINT DISLOCATION ( 9 FDA reports)
LEUKOCYTOSIS ( 9 FDA reports)
MALABSORPTION ( 9 FDA reports)
MELAENA ( 9 FDA reports)
MOVEMENT DISORDER ( 9 FDA reports)
NEUROPATHY PERIPHERAL ( 9 FDA reports)
ORAL PAIN ( 9 FDA reports)
OSTEOARTHRITIS ( 9 FDA reports)
OXYGEN SATURATION DECREASED ( 9 FDA reports)
PAROSMIA ( 9 FDA reports)
RENAL DISORDER ( 9 FDA reports)
RENAL FAILURE ( 9 FDA reports)
SCLERAL DISCOLOURATION ( 9 FDA reports)
SENSORY LOSS ( 9 FDA reports)
TENSION HEADACHE ( 9 FDA reports)
THROAT IRRITATION ( 9 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 9 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 9 FDA reports)
ABDOMINAL TENDERNESS ( 8 FDA reports)
ANAL FISSURE ( 8 FDA reports)
ARRHYTHMIA ( 8 FDA reports)
ASCITES ( 8 FDA reports)
AUTOIMMUNE HEPATITIS ( 8 FDA reports)
BLOOD SODIUM DECREASED ( 8 FDA reports)
CYTOLYTIC HEPATITIS ( 8 FDA reports)
DISORIENTATION ( 8 FDA reports)
DRUG HYPERSENSITIVITY ( 8 FDA reports)
DRY EYE ( 8 FDA reports)
DYSPNOEA EXERTIONAL ( 8 FDA reports)
GENITAL HAEMORRHAGE ( 8 FDA reports)
HAIR DISORDER ( 8 FDA reports)
HEART RATE DECREASED ( 8 FDA reports)
HYSTERECTOMY ( 8 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 8 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 8 FDA reports)
LYMPHADENOPATHY ( 8 FDA reports)
NAIL DISORDER ( 8 FDA reports)
NIGHT SWEATS ( 8 FDA reports)
OBESITY ( 8 FDA reports)
OCULAR ICTERUS ( 8 FDA reports)
PROCTITIS ( 8 FDA reports)
RASH PAPULAR ( 8 FDA reports)
SCAR ( 8 FDA reports)
SKIN DISORDER ( 8 FDA reports)
SNEEZING ( 8 FDA reports)
SPEECH DISORDER ( 8 FDA reports)
STREPTOCOCCAL INFECTION ( 8 FDA reports)
TEMPERATURE REGULATION DISORDER ( 8 FDA reports)
THYROID CANCER ( 8 FDA reports)
TONGUE DISCOLOURATION ( 8 FDA reports)
TONGUE DISORDER ( 8 FDA reports)
URINARY INCONTINENCE ( 8 FDA reports)
ACCIDENTAL EXPOSURE ( 7 FDA reports)
AGITATION ( 7 FDA reports)
BEDRIDDEN ( 7 FDA reports)
BLOOD CREATININE INCREASED ( 7 FDA reports)
BLOOD POTASSIUM INCREASED ( 7 FDA reports)
BLOOD UREA INCREASED ( 7 FDA reports)
BREAST MASS ( 7 FDA reports)
COMA ( 7 FDA reports)
DEPRESSION SUICIDAL ( 7 FDA reports)
EAR PAIN ( 7 FDA reports)
EYE INJURY ( 7 FDA reports)
GINGIVAL PAIN ( 7 FDA reports)
HAEMATOMA ( 7 FDA reports)
HELICOBACTER INFECTION ( 7 FDA reports)
HYPOAESTHESIA ORAL ( 7 FDA reports)
HYPOMETABOLISM ( 7 FDA reports)
INCISION SITE COMPLICATION ( 7 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 7 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 7 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 7 FDA reports)
MOOD SWINGS ( 7 FDA reports)
MOUTH ULCERATION ( 7 FDA reports)
MUSCLE ATROPHY ( 7 FDA reports)
PANCREATIC CARCINOMA ( 7 FDA reports)
PANIC REACTION ( 7 FDA reports)
PROCTITIS ULCERATIVE ( 7 FDA reports)
PULMONARY OEDEMA ( 7 FDA reports)
RECTAL PROLAPSE ( 7 FDA reports)
SEPSIS ( 7 FDA reports)
TONSILLITIS ( 7 FDA reports)
URETHRAL HAEMORRHAGE ( 7 FDA reports)
URINARY TRACT DISORDER ( 7 FDA reports)
ANGER ( 6 FDA reports)
ARTERIOSCLEROSIS ( 6 FDA reports)
BASAL CELL CARCINOMA ( 6 FDA reports)
BILE DUCT OBSTRUCTION ( 6 FDA reports)
BLOOD SODIUM INCREASED ( 6 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 6 FDA reports)
BLOODY DISCHARGE ( 6 FDA reports)
BONE PAIN ( 6 FDA reports)
BRONCHOSPASM ( 6 FDA reports)
CHOLECYSTITIS CHRONIC ( 6 FDA reports)
CHOLECYSTITIS INFECTIVE ( 6 FDA reports)
CHOLESTASIS ( 6 FDA reports)
COLECTOMY ( 6 FDA reports)
DEATH ( 6 FDA reports)
DISABILITY ( 6 FDA reports)
DISTRACTIBILITY ( 6 FDA reports)
ENTEROCOLITIS ( 6 FDA reports)
ESCHERICHIA INFECTION ( 6 FDA reports)
FAECALOMA ( 6 FDA reports)
FIBULA FRACTURE ( 6 FDA reports)
GASTRIC INFECTION ( 6 FDA reports)
GASTROENTERITIS ( 6 FDA reports)
GINGIVAL BLEEDING ( 6 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 6 FDA reports)
HAEMOPTYSIS ( 6 FDA reports)
HAIR TEXTURE ABNORMAL ( 6 FDA reports)
HEPATIC ENCEPHALOPATHY ( 6 FDA reports)
HYPERGLYCAEMIA ( 6 FDA reports)
IMMUNE SYSTEM DISORDER ( 6 FDA reports)
INJURY ( 6 FDA reports)
INTESTINAL HAEMORRHAGE ( 6 FDA reports)
LARGE INTESTINE PERFORATION ( 6 FDA reports)
MUSCLE TWITCHING ( 6 FDA reports)
NEOPLASM ( 6 FDA reports)
OLIGOMENORRHOEA ( 6 FDA reports)
PANCREATIC DISORDER ( 6 FDA reports)
PARANOIA ( 6 FDA reports)
PLEURAL EFFUSION ( 6 FDA reports)
PULMONARY THROMBOSIS ( 6 FDA reports)
RHABDOMYOLYSIS ( 6 FDA reports)
SCREAMING ( 6 FDA reports)
SUFFOCATION FEELING ( 6 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 6 FDA reports)
TENDON RUPTURE ( 6 FDA reports)
TENDONITIS ( 6 FDA reports)
ULCER ( 6 FDA reports)
ULTRASOUND LIVER ( 6 FDA reports)
UPPER LIMB FRACTURE ( 6 FDA reports)
ABDOMINAL RIGIDITY ( 5 FDA reports)
APHASIA ( 5 FDA reports)
APPENDICITIS PERFORATED ( 5 FDA reports)
ASPIRATION ( 5 FDA reports)
BILIARY TRACT DISORDER ( 5 FDA reports)
BILIRUBINURIA ( 5 FDA reports)
BLADDER DISCOMFORT ( 5 FDA reports)
BLADDER DISORDER ( 5 FDA reports)
BLADDER PAIN ( 5 FDA reports)
BLEPHAROSPASM ( 5 FDA reports)
BLOOD VISCOSITY INCREASED ( 5 FDA reports)
BURSITIS ( 5 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 5 FDA reports)
CARDIAC OPERATION ( 5 FDA reports)
COLONIC POLYP ( 5 FDA reports)
DRUG DEPENDENCE ( 5 FDA reports)
DRY THROAT ( 5 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 5 FDA reports)
ELECTROLYTE IMBALANCE ( 5 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 5 FDA reports)
FRACTURE ( 5 FDA reports)
GALLBLADDER OPERATION ( 5 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 5 FDA reports)
GLOMERULONEPHRITIS ( 5 FDA reports)
GOUT ( 5 FDA reports)
HALLUCINATION ( 5 FDA reports)
HEART RATE IRREGULAR ( 5 FDA reports)
HEPATIC CYST ( 5 FDA reports)
HEPATIC PAIN ( 5 FDA reports)
HYPERKERATOSIS ( 5 FDA reports)
HYPOKALAEMIA ( 5 FDA reports)
IMMOBILE ( 5 FDA reports)
IMPAIRED HEALING ( 5 FDA reports)
INCREASED TENDENCY TO BRUISE ( 5 FDA reports)
IRON DEFICIENCY ( 5 FDA reports)
LAPAROSCOPIC SURGERY ( 5 FDA reports)
LIGAMENT RUPTURE ( 5 FDA reports)
LUNG INFECTION ( 5 FDA reports)
LUNG NEOPLASM ( 5 FDA reports)
MEDICAL DIET ( 5 FDA reports)
MENOPAUSE ( 5 FDA reports)
MICTURITION FREQUENCY DECREASED ( 5 FDA reports)
NASAL DISCOMFORT ( 5 FDA reports)
NEUTROPENIA ( 5 FDA reports)
OESOPHAGEAL PAIN ( 5 FDA reports)
ONYCHOCLASIS ( 5 FDA reports)
ORAL MUCOSAL BLISTERING ( 5 FDA reports)
PARALYSIS ( 5 FDA reports)
PELVIC PAIN ( 5 FDA reports)
PERSONALITY CHANGE ( 5 FDA reports)
PHARYNGITIS ( 5 FDA reports)
POST PROCEDURAL COMPLICATION ( 5 FDA reports)
PREGNANCY ( 5 FDA reports)
RIB FRACTURE ( 5 FDA reports)
SKIN BURNING SENSATION ( 5 FDA reports)
SKIN REACTION ( 5 FDA reports)
SKIN ULCER ( 5 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 5 FDA reports)
THROMBOCYTOPENIA ( 5 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 5 FDA reports)
UTERINE PAIN ( 5 FDA reports)
VITAMIN D DECREASED ( 5 FDA reports)
WHEEZING ( 5 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 4 FDA reports)
ANAL FISTULA ( 4 FDA reports)
ANGIOEDEMA ( 4 FDA reports)
ANOSMIA ( 4 FDA reports)
APHAGIA ( 4 FDA reports)
APPENDIX DISORDER ( 4 FDA reports)
ATELECTASIS ( 4 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 4 FDA reports)
BILIARY DYSKINESIA ( 4 FDA reports)
BIOPSY LIVER ( 4 FDA reports)
BLOOD CALCIUM DECREASED ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 4 FDA reports)
BLOOD MAGNESIUM DECREASED ( 4 FDA reports)
BREAST SWELLING ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
CARDIAC MURMUR ( 4 FDA reports)
CHAPPED LIPS ( 4 FDA reports)
CRYSTAL URINE ( 4 FDA reports)
DECREASED ACTIVITY ( 4 FDA reports)
DIVERTICULUM ( 4 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 4 FDA reports)
DRUG ABUSE ( 4 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 4 FDA reports)
DYSPHONIA ( 4 FDA reports)
ECONOMIC PROBLEM ( 4 FDA reports)
ECZEMA ( 4 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 4 FDA reports)
ENTERITIS ( 4 FDA reports)
EOSINOPHIL COUNT INCREASED ( 4 FDA reports)
EYE IRRITATION ( 4 FDA reports)
FACE INJURY ( 4 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 4 FDA reports)
FINGER DEFORMITY ( 4 FDA reports)
GALLBLADDER OEDEMA ( 4 FDA reports)
GASTRIC HAEMORRHAGE ( 4 FDA reports)
GENERALISED OEDEMA ( 4 FDA reports)
HAEMOGLOBIN INCREASED ( 4 FDA reports)
HANGOVER ( 4 FDA reports)
HEPATIC CIRRHOSIS ( 4 FDA reports)
HEPATITIS FULMINANT ( 4 FDA reports)
HEPATO-LENTICULAR DEGENERATION ( 4 FDA reports)
HYPOAESTHESIA FACIAL ( 4 FDA reports)
IMPATIENCE ( 4 FDA reports)
INTENTIONAL OVERDOSE ( 4 FDA reports)
JOINT LOCK ( 4 FDA reports)
MONOCYTE COUNT INCREASED ( 4 FDA reports)
MUSCULOSKELETAL DISORDER ( 4 FDA reports)
MYDRIASIS ( 4 FDA reports)
NIGHTMARE ( 4 FDA reports)
OESOPHAGEAL SPASM ( 4 FDA reports)
OILY SKIN ( 4 FDA reports)
OROPHARYNGEAL BLISTERING ( 4 FDA reports)
PARAESTHESIA ORAL ( 4 FDA reports)
PERICARDIAL EFFUSION ( 4 FDA reports)
PERIPHERAL COLDNESS ( 4 FDA reports)
PLANTAR FASCIITIS ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
PRODUCTIVE COUGH ( 4 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 4 FDA reports)
PRURITUS ANI ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
RECTAL FISSURE ( 4 FDA reports)
RESPIRATORY DISORDER ( 4 FDA reports)
RESPIRATORY DISTRESS ( 4 FDA reports)
RESPIRATORY TRACT INFECTION ( 4 FDA reports)
SALIVARY HYPERSECRETION ( 4 FDA reports)
SCIATICA ( 4 FDA reports)
SENSATION OF FOREIGN BODY ( 4 FDA reports)
SERUM FERRITIN INCREASED ( 4 FDA reports)
SICK SINUS SYNDROME ( 4 FDA reports)
SYNOVIAL CYST ( 4 FDA reports)
TONGUE BITING ( 4 FDA reports)
UNEVALUABLE EVENT ( 4 FDA reports)
VAGINAL PAIN ( 4 FDA reports)
VASCULITIS ( 4 FDA reports)
WISDOM TEETH REMOVAL ( 4 FDA reports)
ABDOMINAL SYMPTOM ( 3 FDA reports)
ABORTION INDUCED ( 3 FDA reports)
ABSCESS ( 3 FDA reports)
AGEUSIA ( 3 FDA reports)
ANAL PRURITUS ( 3 FDA reports)
APHONIA ( 3 FDA reports)
APLASTIC ANAEMIA ( 3 FDA reports)
ARTHROPOD BITE ( 3 FDA reports)
ASTHENOPIA ( 3 FDA reports)
BACTERIAL INFECTION ( 3 FDA reports)
BARRETT'S OESOPHAGUS ( 3 FDA reports)
BLOOD CALCIUM INCREASED ( 3 FDA reports)
BLOOD CREATINE INCREASED ( 3 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 3 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 3 FDA reports)
BODY FAT DISORDER ( 3 FDA reports)
CAROTID ARTERY OCCLUSION ( 3 FDA reports)
CELL DEATH ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
CERVICAL POLYP ( 3 FDA reports)
CHEILITIS ( 3 FDA reports)
CHOLECYSTITIS ACUTE ( 3 FDA reports)
COAGULATION TIME SHORTENED ( 3 FDA reports)
COLON NEOPLASM ( 3 FDA reports)
COLON OPERATION ( 3 FDA reports)
COMMUNICATION DISORDER ( 3 FDA reports)
CYST ( 3 FDA reports)
DEAFNESS UNILATERAL ( 3 FDA reports)
DEEP VEIN THROMBOSIS ( 3 FDA reports)
DERMATITIS ACNEIFORM ( 3 FDA reports)
DERMATITIS BULLOUS ( 3 FDA reports)
DEVELOPMENTAL DELAY ( 3 FDA reports)
DIVERTICULUM INTESTINAL ( 3 FDA reports)
DRUG SCREEN POSITIVE ( 3 FDA reports)
DRUG WITHDRAWAL HEADACHE ( 3 FDA reports)
DUODENAL ULCER ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
ECTOPIC PREGNANCY ( 3 FDA reports)
ENTERITIS INFECTIOUS ( 3 FDA reports)
EOSINOPHILIC OESOPHAGITIS ( 3 FDA reports)
ERECTILE DYSFUNCTION ( 3 FDA reports)
EYE HAEMORRHAGE ( 3 FDA reports)
FLANK PAIN ( 3 FDA reports)
FOOD ALLERGY ( 3 FDA reports)
FOOD AVERSION ( 3 FDA reports)
FOOT OPERATION ( 3 FDA reports)
FORMICATION ( 3 FDA reports)
GALLBLADDER POLYP ( 3 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 3 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 3 FDA reports)
GENITAL DISORDER FEMALE ( 3 FDA reports)
GINGIVAL SWELLING ( 3 FDA reports)
GLOSSODYNIA ( 3 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 3 FDA reports)
GRAND MAL CONVULSION ( 3 FDA reports)
HAEMORRHAGE URINARY TRACT ( 3 FDA reports)
HEARING IMPAIRED ( 3 FDA reports)
HEAT EXHAUSTION ( 3 FDA reports)
HEPATIC ENZYME ABNORMAL ( 3 FDA reports)
HEPATIC LESION ( 3 FDA reports)
HEPATIC NECROSIS ( 3 FDA reports)
HYPERAESTHESIA ( 3 FDA reports)
HYPERMETABOLISM ( 3 FDA reports)
HYPERVENTILATION ( 3 FDA reports)
ILEUS PARALYTIC ( 3 FDA reports)
IMPAIRED WORK ABILITY ( 3 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 3 FDA reports)
INCONTINENCE ( 3 FDA reports)
INFERTILITY ( 3 FDA reports)
INFUSION SITE SWELLING ( 3 FDA reports)
INGUINAL HERNIA ( 3 FDA reports)
INTESTINAL POLYP ( 3 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE EXPELLED ( 3 FDA reports)
KNEE OPERATION ( 3 FDA reports)
LACERATION ( 3 FDA reports)
LACTOSE INTOLERANCE ( 3 FDA reports)
LIP DRY ( 3 FDA reports)
LIPIDS INCREASED ( 3 FDA reports)
LOWER LIMB FRACTURE ( 3 FDA reports)
MANIA ( 3 FDA reports)
METABOLIC DISORDER ( 3 FDA reports)
MOTION SICKNESS ( 3 FDA reports)
MULTIPLE INJURIES ( 3 FDA reports)
MYCOTIC ALLERGY ( 3 FDA reports)
NAIL DISCOLOURATION ( 3 FDA reports)
NARCOLEPSY ( 3 FDA reports)
NASAL DRYNESS ( 3 FDA reports)
NERVE INJURY ( 3 FDA reports)
OESOPHAGITIS ( 3 FDA reports)
ORTHOSTATIC HYPOTENSION ( 3 FDA reports)
OSTEONECROSIS ( 3 FDA reports)
OSTEOPENIA ( 3 FDA reports)
PAIN OF SKIN ( 3 FDA reports)
PAINFUL RESPIRATION ( 3 FDA reports)
PANCREATIC CYST ( 3 FDA reports)
PANCREATITIS CHRONIC ( 3 FDA reports)
PERIORBITAL HAEMATOMA ( 3 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 3 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 3 FDA reports)
PROCEDURAL NAUSEA ( 3 FDA reports)
PRODUCT COUNTERFEIT ( 3 FDA reports)
PROTHROMBIN TIME PROLONGED ( 3 FDA reports)
PSORIASIS ( 3 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 3 FDA reports)
PSYCHOTIC DISORDER ( 3 FDA reports)
PURULENT DISCHARGE ( 3 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 3 FDA reports)
REGURGITATION ( 3 FDA reports)
RENAL INJURY ( 3 FDA reports)
RESTLESS LEGS SYNDROME ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
ROAD TRAFFIC ACCIDENT ( 3 FDA reports)
SIGMOIDECTOMY ( 3 FDA reports)
SINUS CONGESTION ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
SKIN IRRITATION ( 3 FDA reports)
SKIN WRINKLING ( 3 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 3 FDA reports)
SPINAL COMPRESSION FRACTURE ( 3 FDA reports)
SPINAL FRACTURE ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
STRESS FRACTURE ( 3 FDA reports)
TENSION ( 3 FDA reports)
THINKING ABNORMAL ( 3 FDA reports)
TONGUE ULCERATION ( 3 FDA reports)
TOOTH ABSCESS ( 3 FDA reports)
TOOTH EXTRACTION ( 3 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 3 FDA reports)
TRICHORRHEXIS ( 3 FDA reports)
ULCER HAEMORRHAGE ( 3 FDA reports)
ULTRASOUND ABDOMEN ( 3 FDA reports)
ULTRASOUND SCAN ( 3 FDA reports)
UMBILICAL HERNIA ( 3 FDA reports)
UNINTENDED PREGNANCY ( 3 FDA reports)
URINE ANALYSIS ABNORMAL ( 3 FDA reports)
URINE OUTPUT INCREASED ( 3 FDA reports)
VASCULAR INJURY ( 3 FDA reports)
VITAMIN D DEFICIENCY ( 3 FDA reports)
VITAMIN K DEFICIENCY ( 3 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 3 FDA reports)
VULVOVAGINAL DISCOMFORT ( 3 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 3 FDA reports)
WOUND ( 3 FDA reports)
ABDOMEN SCAN ( 2 FDA reports)
ABDOMINAL HERNIA ( 2 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 2 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 2 FDA reports)
ADNEXA UTERI PAIN ( 2 FDA reports)
ALCOHOL USE ( 2 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
ANIMAL BITE ( 2 FDA reports)
ANORECTAL DISORDER ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 2 FDA reports)
AORTIC CALCIFICATION ( 2 FDA reports)
AORTIC VALVE STENOSIS ( 2 FDA reports)
APHTHOUS STOMATITIS ( 2 FDA reports)
ARTHROPOD STING ( 2 FDA reports)
ASTHMATIC CRISIS ( 2 FDA reports)
BASEDOW'S DISEASE ( 2 FDA reports)
BILE DUCT STONE ( 2 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 2 FDA reports)
BIPOLAR DISORDER ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BLEEDING TIME PROLONGED ( 2 FDA reports)
BLOOD INSULIN INCREASED ( 2 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BRAIN STEM STROKE ( 2 FDA reports)
BREAST ATROPHY ( 2 FDA reports)
BREAST CANCER RECURRENT ( 2 FDA reports)
BULIMIA NERVOSA ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARDIAC FLUTTER ( 2 FDA reports)
CARDIAC STRESS TEST ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 2 FDA reports)
CEREBRAL HYPOPERFUSION ( 2 FDA reports)
CHRONIC HEPATITIS ( 2 FDA reports)
COAGULATION TEST ABNORMAL ( 2 FDA reports)
COCCYDYNIA ( 2 FDA reports)
COITAL BLEEDING ( 2 FDA reports)
COLONIC OBSTRUCTION ( 2 FDA reports)
COMPLEMENT FACTOR C3 DECREASED ( 2 FDA reports)
COMPLEX PARTIAL SEIZURES ( 2 FDA reports)
CONCUSSION ( 2 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 2 FDA reports)
CORONARY ARTERY RESTENOSIS ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
CYST REMOVAL ( 2 FDA reports)
CYSTITIS INTERSTITIAL ( 2 FDA reports)
DANDRUFF ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DENTAL PROSTHESIS USER ( 2 FDA reports)
DEREALISATION ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DIABETIC COMA ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DIZZINESS POSTURAL ( 2 FDA reports)
DYSPAREUNIA ( 2 FDA reports)
EAR DISORDER ( 2 FDA reports)
EAR PRURITUS ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
EMERGENCY CARE EXAMINATION ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
ENDODONTIC PROCEDURE ( 2 FDA reports)
ESCHERICHIA SEPSIS ( 2 FDA reports)
EXERCISE LACK OF ( 2 FDA reports)
EYE ROLLING ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FACIAL PALSY ( 2 FDA reports)
FAECAL VOMITING ( 2 FDA reports)
FALLOT'S TETRALOGY ( 2 FDA reports)
FAT INTOLERANCE ( 2 FDA reports)
FEAR OF DEATH ( 2 FDA reports)
FEELING OF RELAXATION ( 2 FDA reports)
FOOD INTOLERANCE ( 2 FDA reports)
FURUNCLE ( 2 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 2 FDA reports)
GASTRIC POLYPS ( 2 FDA reports)
GLOBAL AMNESIA ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMOGLOBIN ABNORMAL ( 2 FDA reports)
HAIR COLOUR CHANGES ( 2 FDA reports)
HEAD DISCOMFORT ( 2 FDA reports)
HEART DISEASE CONGENITAL ( 2 FDA reports)
HEAT RASH ( 2 FDA reports)
HEPATIC FIBROSIS ( 2 FDA reports)
HEPATIC INFECTION ( 2 FDA reports)
HEPATITIS D ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HYDRONEPHROSIS ( 2 FDA reports)
HYDROURETER ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
HYPOVENTILATION ( 2 FDA reports)
IMPAIRED DRIVING ABILITY ( 2 FDA reports)
INCISION SITE INFECTION ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 2 FDA reports)
INTESTINAL CYST ( 2 FDA reports)
INTESTINAL MALROTATION ( 2 FDA reports)
INVESTIGATION ( 2 FDA reports)
JOINT EFFUSION ( 2 FDA reports)
KNEE ARTHROPLASTY ( 2 FDA reports)
LACRIMATION INCREASED ( 2 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 2 FDA reports)
LARGE INTESTINAL ULCER ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LIBIDO INCREASED ( 2 FDA reports)
LIP DISORDER ( 2 FDA reports)
LIPOMA ( 2 FDA reports)
LISTLESS ( 2 FDA reports)
LOSS OF LIBIDO ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
LYMPH NODE PAIN ( 2 FDA reports)
LYMPHOMA ( 2 FDA reports)
MACULAR OEDEMA ( 2 FDA reports)
MAGNETIC RESONANCE CHOLANGIOPANCREATOGRAPHY ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MASKED FACIES ( 2 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
METASTASES TO LYMPH NODES ( 2 FDA reports)
METASTASIS ( 2 FDA reports)
MICTURITION DISORDER ( 2 FDA reports)
MIDDLE EAR EFFUSION ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MOUTH HAEMORRHAGE ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MUSCLE INJURY ( 2 FDA reports)
MUSCLE SWELLING ( 2 FDA reports)
NEPHRECTOMY ( 2 FDA reports)
NEPHROPATHY ( 2 FDA reports)
NEURALGIA ( 2 FDA reports)
NIPPLE PAIN ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 2 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 2 FDA reports)
OBSTRUCTION GASTRIC ( 2 FDA reports)
ODYNOPHAGIA ( 2 FDA reports)
ORAL DISCOMFORT ( 2 FDA reports)
ORAL SURGERY ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
PANCREATIC ENLARGEMENT ( 2 FDA reports)
PARTIAL SEIZURES ( 2 FDA reports)
PERFORMANCE STATUS DECREASED ( 2 FDA reports)
PHARYNGEAL DISORDER ( 2 FDA reports)
PHOBIA ( 2 FDA reports)
PHOTOPSIA ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
PLEURISY ( 2 FDA reports)
POLYCYSTIC OVARIES ( 2 FDA reports)
POST PROCEDURAL SWELLING ( 2 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 2 FDA reports)
PROTEIN TOTAL INCREASED ( 2 FDA reports)
PROTEIN URINE PRESENT ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
RECTAL LESION ( 2 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 2 FDA reports)
RENAL CANCER ( 2 FDA reports)
RENAL CELL CARCINOMA ( 2 FDA reports)
RENAL CYST ( 2 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 2 FDA reports)
RESPIRATORY RATE INCREASED ( 2 FDA reports)
RETINAL DETACHMENT ( 2 FDA reports)
RETINAL HAEMORRHAGE ( 2 FDA reports)
RIGHT ATRIAL DILATATION ( 2 FDA reports)
ROTATOR CUFF SYNDROME ( 2 FDA reports)
SALIVA ALTERED ( 2 FDA reports)
SARCOMA ( 2 FDA reports)
SENSITIVITY OF TEETH ( 2 FDA reports)
SEXUAL DYSFUNCTION ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SIGMOIDITIS ( 2 FDA reports)
SKIN CANCER ( 2 FDA reports)
SKIN WARM ( 2 FDA reports)
SOMNAMBULISM ( 2 FDA reports)
SPINAL DEFORMITY ( 2 FDA reports)
SPLENIC CYST ( 2 FDA reports)
STREPTOCOCCAL IDENTIFICATION TEST POSITIVE ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 2 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 2 FDA reports)
TOBACCO USER ( 2 FDA reports)
TOOTH INFECTION ( 2 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 2 FDA reports)
TROPONIN INCREASED ( 2 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
UTERINE DISORDER ( 2 FDA reports)
VASODILATATION ( 2 FDA reports)
VEIN DISORDER ( 2 FDA reports)
VITAMIN K DECREASED ( 2 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 2 FDA reports)
WHITE BLOOD CELLS URINE ( 2 FDA reports)
WOUND HAEMORRHAGE ( 2 FDA reports)
WRIST FRACTURE ( 2 FDA reports)
X-RAY ABNORMAL ( 2 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABDOMINAL INJURY ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ABORTION MISSED ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ADENOCARCINOMA PANCREAS ( 1 FDA reports)
ADENOMA BENIGN ( 1 FDA reports)
ADHESION ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ALCOHOL INTOLERANCE ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALLERGY TO CHEMICALS ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANAL INJURY ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
APPARENT DEATH ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTERY DISSECTION ( 1 FDA reports)
ARTHROSCOPIC SURGERY ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ASTERIXIS ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BILE OUTPUT ABNORMAL ( 1 FDA reports)
BILE OUTPUT INCREASED ( 1 FDA reports)
BILIARY CIRRHOSIS ( 1 FDA reports)
BILIRUBIN URINE ( 1 FDA reports)
BIOPSY BONE MARROW ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 1 FDA reports)
BLOOD CALCIUM ABNORMAL ( 1 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 1 FDA reports)
BLOOD COUNT ABNORMAL ( 1 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 1 FDA reports)
BLOOD FOLATE INCREASED ( 1 FDA reports)
BLOOD INSULIN DECREASED ( 1 FDA reports)
BLOOD OESTROGEN INCREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD SODIUM ABNORMAL ( 1 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 1 FDA reports)
BLOOD URIC ACID DECREASED ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BLOOD ZINC DECREASED ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BREAST CALCIFICATIONS ( 1 FDA reports)
BREAST CANCER IN SITU ( 1 FDA reports)
BREAST CYST ( 1 FDA reports)
BREAST DISCHARGE ( 1 FDA reports)
BREAST DISCOMFORT ( 1 FDA reports)
BREAST INDURATION ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
BUNION OPERATION ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC FIBRILLATION ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CAROTENE DECREASED ( 1 FDA reports)
CAROTID ENDARTERECTOMY ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CARTILAGE INJURY ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CATHETER PLACEMENT ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CEREBROVASCULAR SPASM ( 1 FDA reports)
CERVICOBRACHIAL SYNDROME ( 1 FDA reports)
CERVIX DISORDER ( 1 FDA reports)
CHEMICAL POISONING ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHONDRITIS ( 1 FDA reports)
CHRONIC FATIGUE SYNDROME ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLOSTOMY ( 1 FDA reports)
CONFUSION POSTOPERATIVE ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 1 FDA reports)
CORNEAL ABRASION ( 1 FDA reports)
CORNEAL EROSION ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CUSHING'S SYNDROME ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CYSTIC FIBROSIS PANCREATIC ( 1 FDA reports)
CYSTITIS NONINFECTIVE ( 1 FDA reports)
CYSTOSCOPY ( 1 FDA reports)
DELUSION OF GRANDEUR ( 1 FDA reports)
DENTAL TREATMENT ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DEVICE MIGRATION ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIAPHRAGMALGIA ( 1 FDA reports)
DIPLEGIA ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DYSENTERY ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
ECHOCARDIOGRAM ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
ELECTIVE SURGERY ( 1 FDA reports)
ELECTROCARDIOGRAM ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELEVATED MOOD ( 1 FDA reports)
ENDOCRINE DISORDER ( 1 FDA reports)
ENDOMETRIOSIS ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EXCESSIVE SKIN ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
EXFOLIATIVE RASH ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE ALLERGY ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
EYELID MARGIN CRUSTING ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
EYELIDS PRURITUS ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FAT NECROSIS ( 1 FDA reports)
FEAR OF EATING ( 1 FDA reports)
FEAR OF WEIGHT GAIN ( 1 FDA reports)
FEELING OF DESPAIR ( 1 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
FUNGAL RASH ( 1 FDA reports)
GALACTORRHOEA ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 1 FDA reports)
GASTRIC BYPASS ( 1 FDA reports)
GASTRIC PERFORATION ( 1 FDA reports)
GASTRIC PH DECREASED ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTRIC ULCER HELICOBACTER ( 1 FDA reports)
GASTROINTESTINAL CARCINOMA ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GASTROINTESTINAL INJURY ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL TRACT MUCOSAL DISCOLOURATION ( 1 FDA reports)
GENITAL RASH ( 1 FDA reports)
GINGIVAL ABSCESS ( 1 FDA reports)
GINGIVAL BLISTER ( 1 FDA reports)
GINGIVAL DISORDER ( 1 FDA reports)
GINGIVAL EROSION ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GLUCOSE URINE PRESENT ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
GRANULOCYTE COUNT DECREASED ( 1 FDA reports)
GRIMACING ( 1 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HALO VISION ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEAT STROKE ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC MASS ( 1 FDA reports)
HEPATITIS A ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATITIS VIRAL ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN ABNORMAL ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HORMONE REPLACEMENT THERAPY ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERAMYLASAEMIA ( 1 FDA reports)
HYPERBILIRUBINAEMIA NEONATAL ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERTRICHOSIS ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
ILEOSTOMY ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
INCISION SITE ABSCESS ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INTERNAL INJURY ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
INTESTINAL MUCOSAL HYPERTROPHY ( 1 FDA reports)
INTESTINAL OPERATION ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
JOINT CREPITATION ( 1 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LABYRINTHITIS ( 1 FDA reports)
LACTATION DISORDER ( 1 FDA reports)
LAGOPHTHALMOS ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 1 FDA reports)
LENTIGO ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
LIGAMENT INJURY ( 1 FDA reports)
LIP EXFOLIATION ( 1 FDA reports)
LIP ULCERATION ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 1 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN ABNORMAL ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
MACROCYTOSIS ( 1 FDA reports)
MALIGNANT FIBROUS HISTIOCYTOMA ( 1 FDA reports)
MALOCCLUSION ( 1 FDA reports)
MASTICATION DISORDER ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MEAN PLATELET VOLUME INCREASED ( 1 FDA reports)
MECHANICAL URTICARIA ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MELANOCYTIC NAEVUS ( 1 FDA reports)
MELANOSIS ( 1 FDA reports)
MENSTRUAL DISCOMFORT ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
MILIA ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MOUTH INJURY ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MUSCLE CONTRACTURE ( 1 FDA reports)
MUSCLE ENZYME INCREASED ( 1 FDA reports)
MUSCLE HYPERTROPHY ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NASAL DISORDER ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
NICOTINE DEPENDENCE ( 1 FDA reports)
NIGHT BLINDNESS ( 1 FDA reports)
NO ADVERSE REACTION ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NON-CARDIAC CHEST PAIN ( 1 FDA reports)
OBSTRUCTION ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OCULAR VASCULAR DISORDER ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA STAGE IV ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL INFECTION ( 1 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 1 FDA reports)
OESOPHAGEAL PAPILLOMA ( 1 FDA reports)
OESOPHAGEAL POLYP ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL DISORDER ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
OVARIAN NEOPLASM ( 1 FDA reports)
PALMAR ERYTHEMA ( 1 FDA reports)
PANCREATIC ENZYMES DECREASED ( 1 FDA reports)
PANCREATIC MASS ( 1 FDA reports)
PANCREATOLITHIASIS ( 1 FDA reports)
PARADOXICAL DRUG REACTION ( 1 FDA reports)
PEAU D'ORANGE ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 1 FDA reports)
PERIANAL ERYTHEMA ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIRECTAL ABSCESS ( 1 FDA reports)
PERITONEAL INFECTION ( 1 FDA reports)
PH URINE DECREASED ( 1 FDA reports)
PHAGOPHOBIA ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
POISONING ( 1 FDA reports)
POLYP ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
POSTNASAL DRIP ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
PRECANCEROUS CELLS PRESENT ( 1 FDA reports)
PRECANCEROUS SKIN LESION ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 1 FDA reports)
PRODUCT LOT NUMBER ISSUE ( 1 FDA reports)
PROSTATOMEGALY ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTRUSION TONGUE ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PSEUDOCYST ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PYURIA ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
REACTIVE PSYCHOSIS ( 1 FDA reports)
RECTAL ABSCESS ( 1 FDA reports)
RECTAL SPASM ( 1 FDA reports)
RECTAL ULCER ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL HAEMORRHAGE ( 1 FDA reports)
RENAL STONE REMOVAL ( 1 FDA reports)
RESIDUAL URINE ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RESPIRATORY TRACT IRRITATION ( 1 FDA reports)
RETROPERITONEAL NEOPLASM ( 1 FDA reports)
ROSACEA ( 1 FDA reports)
SALIVA DISCOLOURATION ( 1 FDA reports)
SALIVARY GLAND DISORDER ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCAR PAIN ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SELF ESTEEM DECREASED ( 1 FDA reports)
SELF-INDUCED VOMITING ( 1 FDA reports)
SEMEN VISCOSITY ( 1 FDA reports)
SENSATION OF PRESSURE ( 1 FDA reports)
SENSE OF OPPRESSION ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SKIN CHAPPED ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SKIN TIGHTNESS ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SLEEP TERROR ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SNORING ( 1 FDA reports)
SOCIAL ALCOHOL DRINKER ( 1 FDA reports)
SOFT TISSUE INJURY ( 1 FDA reports)
SOMATOFORM DISORDER GASTROINTESTINAL ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
STRESS URINARY INCONTINENCE ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SWEAT DISCOLOURATION ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
TENDON INJURY ( 1 FDA reports)
TENOSYNOVITIS ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
TIC ( 1 FDA reports)
TOBACCO ABUSE ( 1 FDA reports)
TONGUE BLISTERING ( 1 FDA reports)
TONGUE COATED ( 1 FDA reports)
TONGUE PARALYSIS ( 1 FDA reports)
TONSILLAR DISORDER ( 1 FDA reports)
TONSILLECTOMY ( 1 FDA reports)
TOOTH DISCOLOURATION ( 1 FDA reports)
TOOTH EROSION ( 1 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 1 FDA reports)
UNDERWEIGHT ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URETHRAL OBSTRUCTION ( 1 FDA reports)
URETHRAL PAIN ( 1 FDA reports)
URETHRAL STENOSIS ( 1 FDA reports)
URINARY LIPIDS PRESENT ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
URINE FLOW DECREASED ( 1 FDA reports)
UTERINE CYST ( 1 FDA reports)
UTERINE HAEMORRHAGE ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
UTERINE PROLAPSE ( 1 FDA reports)
UTERINE SPASM ( 1 FDA reports)
VAGINAL INFECTION ( 1 FDA reports)
VAGINAL INFLAMMATION ( 1 FDA reports)
VAGINAL ODOUR ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
VEIN PAIN ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VIRAL MYOCARDITIS ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
VITAMIN B12 INCREASED ( 1 FDA reports)
VOLUME BLOOD DECREASED ( 1 FDA reports)
VOLVULUS ( 1 FDA reports)
VOMITING IN PREGNANCY ( 1 FDA reports)
VON WILLEBRAND'S DISEASE ( 1 FDA reports)
VULVOVAGINAL PAIN ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)

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