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INFLAMMATORY BOWEL DISEASE ( 45 FDA reports)
ANXIETY ( 42 FDA reports)
COLITIS ULCERATIVE ( 39 FDA reports)
COLITIS ( 33 FDA reports)
DEPRESSION ( 32 FDA reports)
DRUG INEFFECTIVE ( 31 FDA reports)
INSOMNIA ( 30 FDA reports)
GASTROINTESTINAL DISORDER ( 29 FDA reports)
SUICIDAL IDEATION ( 29 FDA reports)
CROHN'S DISEASE ( 21 FDA reports)
IRRITABLE BOWEL SYNDROME ( 20 FDA reports)
DIARRHOEA ( 18 FDA reports)
SOMNOLENCE ( 18 FDA reports)
CONVULSION ( 17 FDA reports)
INTESTINAL OBSTRUCTION ( 17 FDA reports)
BODY DYSMORPHIC DISORDER ( 16 FDA reports)
BULIMIA NERVOSA ( 16 FDA reports)
CELLULITIS ( 16 FDA reports)
CHOLANGITIS SCLEROSING ( 16 FDA reports)
DELUSION ( 16 FDA reports)
HEPATOTOXICITY ( 16 FDA reports)
TYPE 1 DIABETES MELLITUS ( 16 FDA reports)
WEIGHT DECREASED ( 16 FDA reports)
ABDOMINAL PAIN ( 15 FDA reports)
BRONCHITIS ( 15 FDA reports)
CHOLELITHIASIS ( 15 FDA reports)
ENDODONTIC PROCEDURE ( 15 FDA reports)
LIP DRY ( 15 FDA reports)
PANIC ATTACK ( 15 FDA reports)
ALCOHOL ABUSE ( 14 FDA reports)
FATIGUE ( 14 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 14 FDA reports)
PALPITATIONS ( 14 FDA reports)
PRURITUS ( 14 FDA reports)
SLEEP APNOEA SYNDROME ( 14 FDA reports)
ABSCESS LIMB ( 13 FDA reports)
COMA ( 13 FDA reports)
DEPRESSED MOOD ( 13 FDA reports)
KETOACIDOSIS ( 13 FDA reports)
NAUSEA ( 13 FDA reports)
PANCREATITIS CHRONIC ( 13 FDA reports)
PARANOIA ( 13 FDA reports)
RECTAL HAEMORRHAGE ( 13 FDA reports)
SHOULDER OPERATION ( 13 FDA reports)
BLINDNESS ( 12 FDA reports)
ROTATOR CUFF SYNDROME ( 12 FDA reports)
ANAL FISSURE ( 11 FDA reports)
COSTOCHONDRITIS ( 11 FDA reports)
FIBROMYALGIA ( 11 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 11 FDA reports)
MUSCULOSKELETAL DISORDER ( 11 FDA reports)
PEPTIC ULCER ( 11 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 11 FDA reports)
PLEURISY ( 11 FDA reports)
PYREXIA ( 11 FDA reports)
RHINORRHOEA ( 11 FDA reports)
SNEEZING ( 11 FDA reports)
TENDONITIS ( 11 FDA reports)
ULCERATIVE KERATITIS ( 11 FDA reports)
ABDOMINAL PAIN UPPER ( 10 FDA reports)
ADENOIDAL HYPERTROPHY ( 10 FDA reports)
DEATH ( 10 FDA reports)
RHEUMATOID ARTHRITIS ( 10 FDA reports)
TONSILLECTOMY ( 10 FDA reports)
ANAEMIA ( 9 FDA reports)
JOINT INSTABILITY ( 9 FDA reports)
PHARYNGITIS ( 9 FDA reports)
BILE DUCT STENOSIS ( 8 FDA reports)
DIZZINESS ( 8 FDA reports)
DYSPNOEA ( 8 FDA reports)
GASTROENTERITIS ( 8 FDA reports)
VOMITING ( 8 FDA reports)
CHRONIC SINUSITIS ( 7 FDA reports)
COUGH ( 7 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 7 FDA reports)
PNEUMONIA ( 7 FDA reports)
RASH ( 7 FDA reports)
SEPTIC SHOCK ( 7 FDA reports)
ABSCESS NECK ( 6 FDA reports)
ANOREXIA ( 6 FDA reports)
HEPATIC STEATOSIS ( 6 FDA reports)
HYDROCELE ( 6 FDA reports)
HYPERPLASTIC CHOLECYSTOPATHY ( 6 FDA reports)
LYMPHADENITIS ( 6 FDA reports)
OEDEMA ( 6 FDA reports)
REFLUX OESOPHAGITIS ( 6 FDA reports)
SEPSIS NEONATAL ( 6 FDA reports)
SINUSITIS ( 6 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 6 FDA reports)
BLOOD GLUCOSE INCREASED ( 5 FDA reports)
ENTEROCOLITIS ( 5 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 5 FDA reports)
HAEMATOCHEZIA ( 5 FDA reports)
HEPATOMEGALY ( 5 FDA reports)
HYPERTENSION ( 5 FDA reports)
MOTION SICKNESS ( 5 FDA reports)
NO ADVERSE EVENT ( 5 FDA reports)
PREGNANCY ( 5 FDA reports)
PREMATURE BABY ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
THROMBOCYTOPENIA ( 5 FDA reports)
ABORTION INDUCED ( 4 FDA reports)
ACROCHORDON ( 4 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 4 FDA reports)
ACUTE RESPIRATORY FAILURE ( 4 FDA reports)
CHOLECYSTITIS ( 4 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
DRY SKIN ( 4 FDA reports)
ERYTHEMA ( 4 FDA reports)
EYELID DISORDER ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
INGUINAL HERNIA ( 4 FDA reports)
INTERSTITIAL LUNG DISEASE ( 4 FDA reports)
INTESTINAL HAEMORRHAGE ( 4 FDA reports)
JAUNDICE NEONATAL ( 4 FDA reports)
LUNG DISORDER ( 4 FDA reports)
MELANOCYTIC NAEVUS ( 4 FDA reports)
MYASTHENIA GRAVIS ( 4 FDA reports)
NEUTROPENIA ( 4 FDA reports)
NO ADVERSE EFFECT ( 4 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
SKIN PAPILLOMA ( 4 FDA reports)
STOMATITIS ( 4 FDA reports)
UNEVALUABLE EVENT ( 4 FDA reports)
ABDOMINAL MASS ( 3 FDA reports)
APPENDICITIS ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
ATRIAL SEPTAL DEFECT ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 3 FDA reports)
EATING DISORDER ( 3 FDA reports)
GLOMERULONEPHRITIS ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
INFECTION ( 3 FDA reports)
IRON DEFICIENCY ANAEMIA ( 3 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 3 FDA reports)
LARGE INTESTINAL ULCER ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
MENTAL DISORDER ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE ( 3 FDA reports)
OPPORTUNISTIC INFECTION ( 3 FDA reports)
PAIN ( 3 FDA reports)
PARONYCHIA ( 3 FDA reports)
PREMATURE LABOUR ( 3 FDA reports)
STRABISMUS ( 3 FDA reports)
SUDDEN DEATH ( 3 FDA reports)
SWOLLEN TONGUE ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
TOOTH EXTRACTION ( 3 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
ACNE ( 2 FDA reports)
ACUTE LUNG INJURY ( 2 FDA reports)
ACUTE SINUSITIS ( 2 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ARTHROPOD BITE ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BONE GRAFT ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
COXSACKIE VIRAL INFECTION ( 2 FDA reports)
CUTANEOUS VASCULITIS ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DERMATITIS EXFOLIATIVE ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
FAILURE TO THRIVE ( 2 FDA reports)
FALL ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
GALLBLADDER DISORDER ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
GENITAL PRURITUS FEMALE ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HYPERCOAGULATION ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
HYPOVOLAEMIA ( 2 FDA reports)
ILEUS PARALYTIC ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
LIVE BIRTH ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
MALAISE ( 2 FDA reports)
METRORRHAGIA ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
MUSCLE INJURY ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NECK INJURY ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 2 FDA reports)
PARAESTHESIA ORAL ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
POLYP ( 2 FDA reports)
PRE-ECLAMPSIA ( 2 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
PROSTATITIS ( 2 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 2 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 2 FDA reports)
PULSE ABNORMAL ( 2 FDA reports)
RADIATION PNEUMONITIS ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SCAR ( 2 FDA reports)
SKIN INFECTION ( 2 FDA reports)
SKIN IRRITATION ( 2 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 2 FDA reports)
SPUTUM CULTURE POSITIVE ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
TOOTH DISORDER ( 2 FDA reports)
UTERINE CYST ( 2 FDA reports)
VAGINAL BURNING SENSATION ( 2 FDA reports)
VAGINAL SWELLING ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACNE FULMINANS ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 1 FDA reports)
ALCOHOL INTERACTION ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
AMNIORRHOEA ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
ANOXIC ENCEPHALOPATHY ( 1 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ARTHRITIS INFECTIVE ( 1 FDA reports)
ASPERMIA ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
AZOOSPERMIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD FOLATE INCREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRAIN INJURY ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CELL DEATH ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHORIORETINOPATHY ( 1 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COLONIC STENOSIS ( 1 FDA reports)
CONGENITAL HEPATOMEGALY ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEBRILE BONE MARROW APLASIA ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FIBROSARCOMA ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL TOXICITY ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
H1N1 INFLUENZA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBINURIA ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS ALCOHOLIC ( 1 FDA reports)
HIV TEST POSITIVE ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYPERKERATOSIS ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOGEUSIA ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
INCISION SITE BLISTER ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
JAW FRACTURE ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIPOSARCOMA ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MORAXELLA INFECTION ( 1 FDA reports)
MUCOSAL EROSION ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NORMAL NEWBORN ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
PNEUMONIA INFLUENZAL ( 1 FDA reports)
POLYHYDRAMNIOS ( 1 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH ABNORMAL ( 1 FDA reports)
RELAPSING FEVER ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL HAEMORRHAGE ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SINUSITIS FUNGAL ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STILLBIRTH ( 1 FDA reports)
STRESS ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SYNOVIAL CYST ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
TIC ( 1 FDA reports)
TONGUE HAEMATOMA ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 1 FDA reports)
TRANSFUSION MICROCHIMERISM ( 1 FDA reports)
TRANSIENT TACHYPNOEA OF THE NEWBORN ( 1 FDA reports)
TRANSPLANT ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
UNINTENDED PREGNANCY ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VITAMIN B12 INCREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
XEROSIS ( 1 FDA reports)
YELLOW SKIN ( 1 FDA reports)

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