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

INFLAMMATORY BOWEL DISEASE ( 1011 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 815 FDA reports)
DEPRESSION ( 599 FDA reports)
PREGNANCY ( 467 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 457 FDA reports)
COLITIS ULCERATIVE ( 404 FDA reports)
CROHN'S DISEASE ( 396 FDA reports)
ARTHRALGIA ( 345 FDA reports)
DRY SKIN ( 338 FDA reports)
ANXIETY ( 299 FDA reports)
SUICIDAL IDEATION ( 275 FDA reports)
HEADACHE ( 269 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 267 FDA reports)
LIP DRY ( 262 FDA reports)
ABORTION INDUCED ( 248 FDA reports)
IRRITABLE BOWEL SYNDROME ( 201 FDA reports)
MYALGIA ( 162 FDA reports)
COLITIS ( 159 FDA reports)
BACK PAIN ( 155 FDA reports)
ABDOMINAL PAIN ( 151 FDA reports)
INTESTINAL OBSTRUCTION ( 147 FDA reports)
MOOD ALTERED ( 145 FDA reports)
TREATMENT NONCOMPLIANCE ( 131 FDA reports)
EPISTAXIS ( 123 FDA reports)
RECTAL HAEMORRHAGE ( 123 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 122 FDA reports)
ANAEMIA ( 121 FDA reports)
DIARRHOEA ( 119 FDA reports)
FATIGUE ( 119 FDA reports)
NAUSEA ( 117 FDA reports)
RASH ( 111 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 109 FDA reports)
CHAPPED LIPS ( 107 FDA reports)
MOOD SWINGS ( 107 FDA reports)
STRESS ( 99 FDA reports)
VISION BLURRED ( 99 FDA reports)
DRY EYE ( 93 FDA reports)
ACNE ( 91 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 90 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 85 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 85 FDA reports)
IRRITABILITY ( 85 FDA reports)
ABORTION SPONTANEOUS ( 82 FDA reports)
INTESTINAL HAEMORRHAGE ( 78 FDA reports)
GASTROINTESTINAL DISORDER ( 74 FDA reports)
CHEILITIS ( 73 FDA reports)
DRUG INEFFECTIVE ( 73 FDA reports)
ALOPECIA ( 70 FDA reports)
HEPATIC ENZYME INCREASED ( 70 FDA reports)
INSOMNIA ( 69 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 68 FDA reports)
GASTRITIS ( 66 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 64 FDA reports)
DIZZINESS ( 64 FDA reports)
XEROSIS ( 63 FDA reports)
ANAL FISSURE ( 60 FDA reports)
MIGRAINE ( 60 FDA reports)
MATERNAL EXPOSURE BEFORE PREGNANCY ( 58 FDA reports)
DEHYDRATION ( 57 FDA reports)
HAEMATOCHEZIA ( 57 FDA reports)
ANGER ( 56 FDA reports)
AGGRESSION ( 54 FDA reports)
CRYING ( 54 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 54 FDA reports)
DEPRESSED MOOD ( 50 FDA reports)
EMOTIONAL DISTRESS ( 50 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 50 FDA reports)
OEDEMA PERIPHERAL ( 49 FDA reports)
UNINTENDED PREGNANCY ( 46 FDA reports)
CHOLELITHIASIS ( 44 FDA reports)
NO ADVERSE EFFECT ( 44 FDA reports)
ORAL HERPES ( 43 FDA reports)
ABDOMINAL PAIN UPPER ( 42 FDA reports)
APHTHOUS STOMATITIS ( 42 FDA reports)
ARTHRITIS ( 42 FDA reports)
EROSIVE OESOPHAGITIS ( 42 FDA reports)
PRURITUS ( 42 FDA reports)
CHRONIC FATIGUE SYNDROME ( 40 FDA reports)
ECCHYMOSIS ( 40 FDA reports)
HYPOKALAEMIA ( 40 FDA reports)
SINUSITIS ( 40 FDA reports)
PANIC ATTACK ( 39 FDA reports)
VOMITING ( 39 FDA reports)
ABNORMAL BEHAVIOUR ( 38 FDA reports)
CONVULSION ( 38 FDA reports)
HAEMORRHOIDS ( 38 FDA reports)
LIPOMA ( 38 FDA reports)
IRON DEFICIENCY ANAEMIA ( 37 FDA reports)
PAIN ( 37 FDA reports)
ASTHENIA ( 36 FDA reports)
NECK INJURY ( 36 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 36 FDA reports)
LIVER DISORDER ( 35 FDA reports)
NASAL DRYNESS ( 35 FDA reports)
PROCTITIS ( 35 FDA reports)
VAGINAL HAEMORRHAGE ( 35 FDA reports)
DRUG DOSE OMISSION ( 34 FDA reports)
EMOTIONAL DISORDER ( 34 FDA reports)
ADVERSE EVENT ( 33 FDA reports)
OSTEOPENIA ( 33 FDA reports)
CHOLANGITIS SCLEROSING ( 32 FDA reports)
ABDOMINAL DISCOMFORT ( 31 FDA reports)
ERYTHEMA ( 31 FDA reports)
FEELING ABNORMAL ( 31 FDA reports)
WEIGHT DECREASED ( 31 FDA reports)
AGITATION ( 30 FDA reports)
CHEST PAIN ( 30 FDA reports)
DYSPNOEA ( 30 FDA reports)
MUSCULOSKELETAL PAIN ( 30 FDA reports)
OESOPHAGITIS ( 30 FDA reports)
PAIN IN EXTREMITY ( 30 FDA reports)
ECTOPIC PREGNANCY ( 29 FDA reports)
PLATELET COUNT INCREASED ( 29 FDA reports)
SUICIDE ATTEMPT ( 29 FDA reports)
LYMPHADENOPATHY ( 28 FDA reports)
ILEITIS ( 27 FDA reports)
PREGNANCY TEST FALSE POSITIVE ( 27 FDA reports)
PSEUDOPOLYP ( 27 FDA reports)
SACROILIITIS ( 27 FDA reports)
TINNITUS ( 27 FDA reports)
DEATH ( 26 FDA reports)
DISTURBANCE IN ATTENTION ( 26 FDA reports)
ECZEMA ( 26 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 26 FDA reports)
MALAISE ( 26 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 26 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 25 FDA reports)
ABSCESS ( 24 FDA reports)
COLON INJURY ( 24 FDA reports)
COLONIC STENOSIS ( 24 FDA reports)
ILEUS ( 24 FDA reports)
NASOPHARYNGITIS ( 24 FDA reports)
DECREASED APPETITE ( 23 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 23 FDA reports)
EDUCATIONAL PROBLEM ( 23 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 23 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 22 FDA reports)
GASTROENTERITIS ( 22 FDA reports)
ILL-DEFINED DISORDER ( 22 FDA reports)
INJURY ( 22 FDA reports)
SCAR ( 22 FDA reports)
SUNBURN ( 22 FDA reports)
VIRAL INFECTION ( 22 FDA reports)
VISUAL ACUITY REDUCED ( 22 FDA reports)
COUGH ( 21 FDA reports)
ILEAL STENOSIS ( 21 FDA reports)
PEPTIC ULCER ( 21 FDA reports)
URTICARIA ( 21 FDA reports)
HAEMORRHAGE ( 20 FDA reports)
CONSTIPATION ( 19 FDA reports)
LIVE BIRTH ( 19 FDA reports)
PYREXIA ( 19 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 18 FDA reports)
GASTROINTESTINAL INJURY ( 18 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 18 FDA reports)
MYOCARDIAL INFARCTION ( 18 FDA reports)
SOMNOLENCE ( 18 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 18 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 17 FDA reports)
BRONCHITIS ( 17 FDA reports)
COMPLETED SUICIDE ( 17 FDA reports)
CONDITION AGGRAVATED ( 17 FDA reports)
DRUG INTOLERANCE ( 17 FDA reports)
DRY MOUTH ( 17 FDA reports)
HERPES ZOSTER ( 17 FDA reports)
HYPERSENSITIVITY ( 17 FDA reports)
INTENTIONAL SELF-INJURY ( 17 FDA reports)
JAUNDICE ( 17 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 17 FDA reports)
PALPITATIONS ( 17 FDA reports)
PARONYCHIA ( 17 FDA reports)
PREGNANCY OF PARTNER ( 17 FDA reports)
PREGNANCY ON CONTRACEPTIVE ( 17 FDA reports)
PROCTITIS ULCERATIVE ( 17 FDA reports)
PULMONARY EMBOLISM ( 17 FDA reports)
RASH PRURITIC ( 17 FDA reports)
RHEUMATOID ARTHRITIS ( 17 FDA reports)
VARICELLA ( 17 FDA reports)
ANAL FISTULA ( 16 FDA reports)
CARCINOID TUMOUR ( 16 FDA reports)
CARDIAC MURMUR ( 16 FDA reports)
GASTRIC ULCER ( 16 FDA reports)
HAEMANGIOMA OF LIVER ( 16 FDA reports)
MENTAL DISORDER ( 16 FDA reports)
NEPHROLITHIASIS ( 16 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 16 FDA reports)
SYNCOPE ( 16 FDA reports)
ACNE CYSTIC ( 15 FDA reports)
DEEP VEIN THROMBOSIS ( 15 FDA reports)
FUNGAL INFECTION ( 15 FDA reports)
HYPOAESTHESIA ( 15 FDA reports)
IMPETIGO ( 15 FDA reports)
LIPIDS INCREASED ( 15 FDA reports)
NECK PAIN ( 15 FDA reports)
SKIN PAPILLOMA ( 15 FDA reports)
VISUAL IMPAIRMENT ( 15 FDA reports)
AFFECT LABILITY ( 14 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 14 FDA reports)
CHEST DISCOMFORT ( 14 FDA reports)
COLITIS COLLAGENOUS ( 14 FDA reports)
DYSPHAGIA ( 14 FDA reports)
ECTOPIC PREGNANCY TERMINATION ( 14 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 14 FDA reports)
METRORRHAGIA ( 14 FDA reports)
PELVIC ABSCESS ( 14 FDA reports)
PHOTOSENSITIVITY REACTION ( 14 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 14 FDA reports)
GAIT DISTURBANCE ( 13 FDA reports)
LETHARGY ( 13 FDA reports)
MAJOR DEPRESSION ( 13 FDA reports)
NIGHT BLINDNESS ( 13 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 13 FDA reports)
OVARIAN CYST ( 13 FDA reports)
ANAL ABSCESS ( 12 FDA reports)
ANGIOKERATOMA ( 12 FDA reports)
ANOREXIA ( 12 FDA reports)
DRUG HYPERSENSITIVITY ( 12 FDA reports)
GASTROINTESTINAL OEDEMA ( 12 FDA reports)
HYPERGLYCAEMIA ( 12 FDA reports)
INFLUENZA ( 12 FDA reports)
MULTI-ORGAN DISORDER ( 12 FDA reports)
MUSCLE SPASMS ( 12 FDA reports)
PANCREATITIS ( 12 FDA reports)
PYELONEPHRITIS ACUTE ( 12 FDA reports)
SINUS HEADACHE ( 12 FDA reports)
SUBCUTANEOUS ABSCESS ( 12 FDA reports)
VOLVULUS ( 12 FDA reports)
AMNESIA ( 11 FDA reports)
ANHEDONIA ( 11 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 11 FDA reports)
BLOOD PRESSURE INCREASED ( 11 FDA reports)
DRUG EFFECT DECREASED ( 11 FDA reports)
GASTRIC DISORDER ( 11 FDA reports)
GOITRE ( 11 FDA reports)
HYPOTHYROIDISM ( 11 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 11 FDA reports)
LOSS OF CONSCIOUSNESS ( 11 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 11 FDA reports)
NEUTROPHIL COUNT INCREASED ( 11 FDA reports)
PERSONALITY CHANGE ( 11 FDA reports)
PROTEINURIA ( 11 FDA reports)
PYODERMA GANGRENOSUM ( 11 FDA reports)
QUALITY OF LIFE DECREASED ( 11 FDA reports)
URINARY TRACT INFECTION ( 11 FDA reports)
BIPOLAR DISORDER ( 10 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 10 FDA reports)
DERMATITIS CONTACT ( 10 FDA reports)
EAR PAIN ( 10 FDA reports)
GUN SHOT WOUND ( 10 FDA reports)
HALLUCINATION ( 10 FDA reports)
HALLUCINATION, AUDITORY ( 10 FDA reports)
HEART RATE INCREASED ( 10 FDA reports)
INGROWING NAIL ( 10 FDA reports)
INTESTINAL PERFORATION ( 10 FDA reports)
LEUKOPENIA ( 10 FDA reports)
MEMORY IMPAIRMENT ( 10 FDA reports)
MUSCULOSKELETAL DISORDER ( 10 FDA reports)
NO ADVERSE EVENT ( 10 FDA reports)
OESOPHAGEAL ULCER ( 10 FDA reports)
OROPHARYNGEAL PAIN ( 10 FDA reports)
RASH MACULAR ( 10 FDA reports)
SKIN DISCOLOURATION ( 10 FDA reports)
VERTIGO ( 10 FDA reports)
APATHY ( 9 FDA reports)
BRAIN NEOPLASM ( 9 FDA reports)
BURNING SENSATION ( 9 FDA reports)
DISCOMFORT ( 9 FDA reports)
DYSURIA ( 9 FDA reports)
EYE IRRITATION ( 9 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 9 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 9 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 9 FDA reports)
INTESTINAL STENOSIS ( 9 FDA reports)
LABORATORY TEST ABNORMAL ( 9 FDA reports)
NORMAL NEWBORN ( 9 FDA reports)
PERICARDITIS ( 9 FDA reports)
PHARYNGEAL OEDEMA ( 9 FDA reports)
PLATELET COUNT DECREASED ( 9 FDA reports)
SELF-INJURIOUS IDEATION ( 9 FDA reports)
TONSILLAR HYPERTROPHY ( 9 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 9 FDA reports)
ABDOMINAL ABSCESS ( 8 FDA reports)
ABDOMINAL DISTENSION ( 8 FDA reports)
ABNORMAL DREAMS ( 8 FDA reports)
AMENORRHOEA ( 8 FDA reports)
CONFUSIONAL STATE ( 8 FDA reports)
DECREASED INTEREST ( 8 FDA reports)
EXTERNAL EAR CELLULITIS ( 8 FDA reports)
EYE PAIN ( 8 FDA reports)
FALL ( 8 FDA reports)
FIBROMYALGIA ( 8 FDA reports)
FURUNCLE ( 8 FDA reports)
GASTRITIS EROSIVE ( 8 FDA reports)
HORDEOLUM ( 8 FDA reports)
HYPERHIDROSIS ( 8 FDA reports)
JOINT STIFFNESS ( 8 FDA reports)
LIP SWELLING ( 8 FDA reports)
LUPUS-LIKE SYNDROME ( 8 FDA reports)
MOLLUSCUM CONTAGIOSUM ( 8 FDA reports)
NEOPLASM MALIGNANT ( 8 FDA reports)
OFF LABEL USE ( 8 FDA reports)
PARAESTHESIA ( 8 FDA reports)
PARANOIA ( 8 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 8 FDA reports)
PHARYNGEAL ULCERATION ( 8 FDA reports)
PHARYNGITIS ( 8 FDA reports)
PSORIASIS ( 8 FDA reports)
PSYCHOTIC DISORDER ( 8 FDA reports)
RHINITIS ALLERGIC ( 8 FDA reports)
SKIN IRRITATION ( 8 FDA reports)
SLEEP DISORDER ( 8 FDA reports)
SWELLING FACE ( 8 FDA reports)
TINEA INFECTION ( 8 FDA reports)
ANKLE FRACTURE ( 7 FDA reports)
AUTOIMMUNE HEPATITIS ( 7 FDA reports)
BLOOD IRON DECREASED ( 7 FDA reports)
CARDIOVASCULAR DISORDER ( 7 FDA reports)
DEAFNESS ( 7 FDA reports)
DERMATITIS ( 7 FDA reports)
DIVERTICULITIS ( 7 FDA reports)
DIVERTICULUM ( 7 FDA reports)
DRUG INTERACTION ( 7 FDA reports)
DYSPEPSIA ( 7 FDA reports)
FEAR ( 7 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 7 FDA reports)
HEPATOCELLULAR DAMAGE ( 7 FDA reports)
HYPERTENSION ( 7 FDA reports)
HYSTERECTOMY ( 7 FDA reports)
IMMUNE SYSTEM DISORDER ( 7 FDA reports)
INTESTINAL FISTULA ( 7 FDA reports)
LARYNGITIS ( 7 FDA reports)
MENSTRUATION IRREGULAR ( 7 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 7 FDA reports)
NEUROBLASTOMA ( 7 FDA reports)
OCULAR HYPERAEMIA ( 7 FDA reports)
PAPILLOEDEMA ( 7 FDA reports)
SPLENOMEGALY ( 7 FDA reports)
STAPHYLOCOCCAL INFECTION ( 7 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 7 FDA reports)
TESTIS CANCER ( 7 FDA reports)
THROMBOSIS ( 7 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 7 FDA reports)
VOCAL CORD CYST ( 7 FDA reports)
ACNE FULMINANS ( 6 FDA reports)
ADENOMA BENIGN ( 6 FDA reports)
AFFECTIVE DISORDER ( 6 FDA reports)
APPENDICITIS ( 6 FDA reports)
BLIGHTED OVUM ( 6 FDA reports)
DISEASE RECURRENCE ( 6 FDA reports)
ELBOW OPERATION ( 6 FDA reports)
FAECES DISCOLOURED ( 6 FDA reports)
FLATULENCE ( 6 FDA reports)
FOLLICULITIS ( 6 FDA reports)
GALLBLADDER DISORDER ( 6 FDA reports)
GASTROENTERITIS VIRAL ( 6 FDA reports)
HYPERLIPIDAEMIA ( 6 FDA reports)
HYPERSOMNIA ( 6 FDA reports)
IMPAIRED HEALING ( 6 FDA reports)
INGROWN HAIR ( 6 FDA reports)
INTERNAL INJURY ( 6 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 6 FDA reports)
LARGE INTESTINE PERFORATION ( 6 FDA reports)
MELANOCYTIC NAEVUS ( 6 FDA reports)
MITRAL VALVE PROLAPSE ( 6 FDA reports)
MONONUCLEOSIS SYNDROME ( 6 FDA reports)
MUSCULAR WEAKNESS ( 6 FDA reports)
NERVOUSNESS ( 6 FDA reports)
OPTIC NERVE DISORDER ( 6 FDA reports)
POUCHITIS ( 6 FDA reports)
PREGNANCY TEST POSITIVE ( 6 FDA reports)
SKIN LACERATION ( 6 FDA reports)
SKIN MASS ( 6 FDA reports)
STREPTOCOCCAL INFECTION ( 6 FDA reports)
TRANSAMINASES INCREASED ( 6 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 6 FDA reports)
WISDOM TEETH REMOVAL ( 6 FDA reports)
ABORTION ( 5 FDA reports)
ACCIDENTAL OVERDOSE ( 5 FDA reports)
ADVERSE REACTION ( 5 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 5 FDA reports)
ANTISOCIAL BEHAVIOUR ( 5 FDA reports)
BLOOD BILIRUBIN INCREASED ( 5 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 5 FDA reports)
BONE PAIN ( 5 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 5 FDA reports)
CHILLS ( 5 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 5 FDA reports)
DEPRESSIVE SYMPTOM ( 5 FDA reports)
DYSPNOEA EXERTIONAL ( 5 FDA reports)
EXCORIATION ( 5 FDA reports)
FAMILY STRESS ( 5 FDA reports)
FEELING OF DESPAIR ( 5 FDA reports)
FISTULA ( 5 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 5 FDA reports)
GENITAL LESION ( 5 FDA reports)
HALLUCINATION, VISUAL ( 5 FDA reports)
HOMICIDAL IDEATION ( 5 FDA reports)
HYDRONEPHROSIS ( 5 FDA reports)
INFECTED CYST ( 5 FDA reports)
INFLUENZA LIKE ILLNESS ( 5 FDA reports)
INTENTIONAL OVERDOSE ( 5 FDA reports)
LIBIDO DECREASED ( 5 FDA reports)
LIGAMENT RUPTURE ( 5 FDA reports)
LIP HAEMORRHAGE ( 5 FDA reports)
LIP OEDEMA ( 5 FDA reports)
LOCAL SWELLING ( 5 FDA reports)
LYMPHOMA ( 5 FDA reports)
MILIA ( 5 FDA reports)
MUCOSAL DRYNESS ( 5 FDA reports)
NEOPLASM PROGRESSION ( 5 FDA reports)
NEUTROPENIA ( 5 FDA reports)
OOPHORECTOMY ( 5 FDA reports)
PHOTOPHOBIA ( 5 FDA reports)
PHOTOPSIA ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
POLLAKIURIA ( 5 FDA reports)
RASH ERYTHEMATOUS ( 5 FDA reports)
RECTAL ABSCESS ( 5 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
RESTLESSNESS ( 5 FDA reports)
SCAR EXCISION ( 5 FDA reports)
SCIATICA ( 5 FDA reports)
SKIN EXFOLIATION ( 5 FDA reports)
SKIN FISSURES ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
TENDONITIS ( 5 FDA reports)
TONSILLITIS ( 5 FDA reports)
TRANSFUSION ( 5 FDA reports)
UNWANTED PREGNANCY ( 5 FDA reports)
UPPER LIMB FRACTURE ( 5 FDA reports)
WEIGHT INCREASED ( 5 FDA reports)
ABNORMAL SENSATION IN EYE ( 4 FDA reports)
ACARODERMATITIS ( 4 FDA reports)
ASTHMA ( 4 FDA reports)
BLOOD CALCIUM INCREASED ( 4 FDA reports)
COELIAC DISEASE ( 4 FDA reports)
CONTUSION ( 4 FDA reports)
COSTOCHONDRITIS ( 4 FDA reports)
DEAFNESS UNILATERAL ( 4 FDA reports)
DEFAECATION URGENCY ( 4 FDA reports)
DEPRESSION SUICIDAL ( 4 FDA reports)
DERMAL CYST ( 4 FDA reports)
DRY THROAT ( 4 FDA reports)
DUODENITIS ( 4 FDA reports)
DYSMENORRHOEA ( 4 FDA reports)
DYSPHONIA ( 4 FDA reports)
ECZEMA NUMMULAR ( 4 FDA reports)
EYE PRURITUS ( 4 FDA reports)
EYE SWELLING ( 4 FDA reports)
FACE INJURY ( 4 FDA reports)
FEMALE REPRODUCTIVE NEOPLASM ( 4 FDA reports)
FLAT AFFECT ( 4 FDA reports)
FRACTURE ( 4 FDA reports)
GALLBLADDER POLYP ( 4 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 4 FDA reports)
GENITAL HERPES ( 4 FDA reports)
GLIOBLASTOMA ( 4 FDA reports)
GROIN PAIN ( 4 FDA reports)
HEPATIC PAIN ( 4 FDA reports)
HEPATIC STEATOSIS ( 4 FDA reports)
HIDRADENITIS ( 4 FDA reports)
HOSPITALISATION ( 4 FDA reports)
HYPERCHOLESTEROLAEMIA ( 4 FDA reports)
HYPOAESTHESIA FACIAL ( 4 FDA reports)
INFLAMMATION ( 4 FDA reports)
INTESTINAL RESECTION ( 4 FDA reports)
IRREGULAR SLEEP PHASE ( 4 FDA reports)
JOINT SWELLING ( 4 FDA reports)
LIP EXFOLIATION ( 4 FDA reports)
LOSS OF EMPLOYMENT ( 4 FDA reports)
LUNG NEOPLASM MALIGNANT ( 4 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 4 FDA reports)
MENTAL IMPAIRMENT ( 4 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 4 FDA reports)
NIGHT SWEATS ( 4 FDA reports)
NODULE ( 4 FDA reports)
OCULAR DISCOMFORT ( 4 FDA reports)
OEDEMA ( 4 FDA reports)
OPTIC NEURITIS ( 4 FDA reports)
OSTEOARTHRITIS ( 4 FDA reports)
OVERDOSE ( 4 FDA reports)
PAIN OF SKIN ( 4 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 4 FDA reports)
PILONIDAL CYST ( 4 FDA reports)
PNEUMONIA MYCOPLASMAL ( 4 FDA reports)
RASH PUSTULAR ( 4 FDA reports)
RENAL DISORDER ( 4 FDA reports)
SKIN TIGHTNESS ( 4 FDA reports)
SPECIFIC GRAVITY URINE INCREASED ( 4 FDA reports)
STOMACH DISCOMFORT ( 4 FDA reports)
STOMATITIS ( 4 FDA reports)
TENDON PAIN ( 4 FDA reports)
THINKING ABNORMAL ( 4 FDA reports)
TINEA PEDIS ( 4 FDA reports)
TOOTH EXTRACTION ( 4 FDA reports)
ULCER ( 4 FDA reports)
URETHRITIS NONINFECTIVE ( 4 FDA reports)
VISUAL DISTURBANCE ( 4 FDA reports)
VISUAL FIELD DEFECT ( 4 FDA reports)
VULVOVAGINAL DRYNESS ( 4 FDA reports)
ABORTION INDUCED COMPLETE ( 3 FDA reports)
ACCIDENTAL EXPOSURE ( 3 FDA reports)
ANGIOEDEMA ( 3 FDA reports)
APPENDICECTOMY ( 3 FDA reports)
ARTHRITIS INFECTIVE ( 3 FDA reports)
BASAL CELL CARCINOMA ( 3 FDA reports)
BLISTER ( 3 FDA reports)
BLOOD URINE PRESENT ( 3 FDA reports)
BREAST CANCER FEMALE ( 3 FDA reports)
BREECH PRESENTATION ( 3 FDA reports)
CAESAREAN SECTION ( 3 FDA reports)
CHOLECYSTITIS ( 3 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 3 FDA reports)
CONJUNCTIVITIS ( 3 FDA reports)
CYST ( 3 FDA reports)
CYSTITIS ( 3 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 3 FDA reports)
DEVICE BREAKAGE ( 3 FDA reports)
DEVICE FAILURE ( 3 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 3 FDA reports)
DRUG DISPENSING ERROR ( 3 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 3 FDA reports)
EAR INFECTION ( 3 FDA reports)
ECONOMIC PROBLEM ( 3 FDA reports)
ENTEROBACTER INFECTION ( 3 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 3 FDA reports)
ERYTHEMA NODOSUM ( 3 FDA reports)
EYELID BLEEDING ( 3 FDA reports)
EYELID OEDEMA ( 3 FDA reports)
FACIAL PAIN ( 3 FDA reports)
FLIGHT OF IDEAS ( 3 FDA reports)
FOOD INTOLERANCE ( 3 FDA reports)
FOOT FRACTURE ( 3 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 3 FDA reports)
GASTRIC ULCER PERFORATION ( 3 FDA reports)
GLIOBLASTOMA MULTIFORME ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
HAEMATOMA ( 3 FDA reports)
HAEMATURIA ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HEAD INJURY ( 3 FDA reports)
HEARING IMPAIRED ( 3 FDA reports)
HEPATITIS ( 3 FDA reports)
HIATUS HERNIA ( 3 FDA reports)
HISTOPLASMOSIS ( 3 FDA reports)
IMPAIRED WORK ABILITY ( 3 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 3 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 3 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 3 FDA reports)
LHERMITTE'S SIGN ( 3 FDA reports)
LIP DISCOLOURATION ( 3 FDA reports)
LOCALISED INFECTION ( 3 FDA reports)
LOWER LIMB FRACTURE ( 3 FDA reports)
LYMPHOPENIA ( 3 FDA reports)
MALE CONTRACEPTION ( 3 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 3 FDA reports)
MENISCUS LESION ( 3 FDA reports)
MENORRHAGIA ( 3 FDA reports)
MENTAL STATUS CHANGES ( 3 FDA reports)
MOBILITY DECREASED ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE ( 3 FDA reports)
MUSCLE TIGHTNESS ( 3 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 3 FDA reports)
NEOPLASM RECURRENCE ( 3 FDA reports)
NIGHTMARE ( 3 FDA reports)
OTITIS MEDIA ( 3 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 3 FDA reports)
POLYTRAUMATISM ( 3 FDA reports)
POST CONCUSSION SYNDROME ( 3 FDA reports)
POST PROCEDURAL COMPLICATION ( 3 FDA reports)
PREGNANCY TEST URINE POSITIVE ( 3 FDA reports)
PREMATURE LABOUR ( 3 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 3 FDA reports)
RECURRENT CANCER ( 3 FDA reports)
ROAD TRAFFIC ACCIDENT ( 3 FDA reports)
ROSACEA ( 3 FDA reports)
SCAB ( 3 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 3 FDA reports)
SELF-MEDICATION ( 3 FDA reports)
SENSORY LOSS ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
SKIN INJURY ( 3 FDA reports)
SKIN REACTION ( 3 FDA reports)
SPEECH DISORDER ( 3 FDA reports)
STILLBIRTH ( 3 FDA reports)
SURGERY ( 3 FDA reports)
SWELLING ( 3 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 3 FDA reports)
THERAPY NON-RESPONDER ( 3 FDA reports)
THYROID CANCER ( 3 FDA reports)
TRANSIENT ACANTHOLYTIC DERMATOSIS ( 3 FDA reports)
TRICHORRHEXIS ( 3 FDA reports)
ULCERATIVE KERATITIS ( 3 FDA reports)
UNEVALUABLE EVENT ( 3 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 3 FDA reports)
VAGINITIS BACTERIAL ( 3 FDA reports)
VITAMIN A INCREASED ( 3 FDA reports)
VOCAL CORD DISORDER ( 3 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 3 FDA reports)
ADRENAL CYST ( 2 FDA reports)
ANKYLOSING SPONDYLITIS ( 2 FDA reports)
ARTHRITIS ENTEROPATHIC ( 2 FDA reports)
ATRIAL TACHYCARDIA ( 2 FDA reports)
AURICULAR SWELLING ( 2 FDA reports)
AUTOMATISM ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BARRETT'S OESOPHAGUS ( 2 FDA reports)
BEDRIDDEN ( 2 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 2 FDA reports)
BONE DISORDER ( 2 FDA reports)
BRAIN MASS ( 2 FDA reports)
BURSITIS ( 2 FDA reports)
CARBUNCLE ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CHROMATURIA ( 2 FDA reports)
CHRONIC SINUSITIS ( 2 FDA reports)
COLITIS MICROSCOPIC ( 2 FDA reports)
COLONIC POLYP ( 2 FDA reports)
CONCUSSION ( 2 FDA reports)
CONGENITAL BLADDER ANOMALY ( 2 FDA reports)
CSF PRESSURE INCREASED ( 2 FDA reports)
CULTURE WOUND POSITIVE ( 2 FDA reports)
DECREASED ACTIVITY ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DERMATITIS ACNEIFORM ( 2 FDA reports)
DEVICE RELATED INFECTION ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DIVERTICULAR PERFORATION ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
DYSPAREUNIA ( 2 FDA reports)
EAR DISORDER ( 2 FDA reports)
ENTERITIS ( 2 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 2 FDA reports)
EPIPHYSES PREMATURE FUSION ( 2 FDA reports)
ERECTILE DYSFUNCTION ( 2 FDA reports)
ERUCTATION ( 2 FDA reports)
ERYTHEMA INFECTIOSUM ( 2 FDA reports)
EXPOSURE VIA FATHER ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
EYE LASER SURGERY ( 2 FDA reports)
FACIAL ASYMMETRY ( 2 FDA reports)
FOOD POISONING ( 2 FDA reports)
GASTROINTESTINAL PAIN ( 2 FDA reports)
GENITAL HAEMORRHAGE ( 2 FDA reports)
GENITAL PAIN ( 2 FDA reports)
GLOMERULONEPHRITIS ( 2 FDA reports)
GOUT ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
GROWTH RETARDATION ( 2 FDA reports)
HAEMANGIOMA CONGENITAL ( 2 FDA reports)
HAEMATOCRIT ABNORMAL ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMOGLOBINOPATHY ( 2 FDA reports)
HAIR TEXTURE ABNORMAL ( 2 FDA reports)
HEART DISEASE CONGENITAL ( 2 FDA reports)
HEPATIC ENZYME ABNORMAL ( 2 FDA reports)
HEPATITIS C ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
HOSTILITY ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYDROCEPHALUS ( 2 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 2 FDA reports)
HYPERVITAMINOSIS ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
IMPAIRED SELF-CARE ( 2 FDA reports)
IMPULSE-CONTROL DISORDER ( 2 FDA reports)
IMPULSIVE BEHAVIOUR ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INCREASED APPETITE ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INTRACRANIAL HYPOTENSION ( 2 FDA reports)
IRON DEFICIENCY ( 2 FDA reports)
JOINT INJURY ( 2 FDA reports)
KERATITIS VIRAL ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
LAZINESS ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LICHEN PLANUS ( 2 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MENSTRUAL DISORDER ( 2 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
MOUTH ULCERATION ( 2 FDA reports)
MUSCLE FATIGUE ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
NASAL POLYPS ( 2 FDA reports)
NEGATIVE THOUGHTS ( 2 FDA reports)
NEONATAL ASPIRATION ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 2 FDA reports)
NO ADVERSE DRUG EFFECT ( 2 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 2 FDA reports)
OBSESSIVE THOUGHTS ( 2 FDA reports)
OESOPHAGEAL ACHALASIA ( 2 FDA reports)
OESOPHAGEAL STENOSIS ( 2 FDA reports)
OLIGOHYDRAMNIOS ( 2 FDA reports)
PARENT-CHILD PROBLEM ( 2 FDA reports)
PELVIC PAIN ( 2 FDA reports)
PENILE HAEMORRHAGE ( 2 FDA reports)
POISONING ( 2 FDA reports)
POLYP ( 2 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 2 FDA reports)
PREGNANCY AFTER POST COITAL CONTRACEPTION ( 2 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 2 FDA reports)
PREGNANCY WITH INJECTABLE CONTRACEPTIVE ( 2 FDA reports)
PROCTALGIA ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
PSYCHIATRIC SYMPTOM ( 2 FDA reports)
PSYCHOTIC BEHAVIOUR ( 2 FDA reports)
PULMONARY HYPOPLASIA ( 2 FDA reports)
PULMONARY INFARCTION ( 2 FDA reports)
PULMONARY MASS ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SINUS CONGESTION ( 2 FDA reports)
SKIN BURNING SENSATION ( 2 FDA reports)
SKIN CHAPPED ( 2 FDA reports)
SKIN HAEMORRHAGE ( 2 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 2 FDA reports)
SPINAL FRACTURE ( 2 FDA reports)
SQUAMOUS CELL CARCINOMA ( 2 FDA reports)
SQUAMOUS CELL CARCINOMA OF THE CERVIX ( 2 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 2 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 2 FDA reports)
TEARFULNESS ( 2 FDA reports)
TEMPERATURE INTOLERANCE ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
THYROID DISORDER ( 2 FDA reports)
TONSILLECTOMY ( 2 FDA reports)
TOOTH ABSCESS ( 2 FDA reports)
TREATMENT FAILURE ( 2 FDA reports)
TREMOR ( 2 FDA reports)
TUNNEL VISION ( 2 FDA reports)
URINARY TRACT DISORDER ( 2 FDA reports)
UTERINE LEIOMYOMA ( 2 FDA reports)
VAGINAL DISCHARGE ( 2 FDA reports)
VAGINAL INFECTION ( 2 FDA reports)
VASCULITIS ( 2 FDA reports)
VITAMIN D DECREASED ( 2 FDA reports)
VOCAL CORD INFLAMMATION ( 2 FDA reports)
WEIGHT FLUCTUATION ( 2 FDA reports)
WITHDRAWAL SYNDROME ( 2 FDA reports)
WOUND INFECTION ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 1 FDA reports)
ABORTION INCOMPLETE ( 1 FDA reports)
ABORTION MISSED ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE STRESS DISORDER ( 1 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ANAL DISCOMFORT ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 1 FDA reports)
ANKLE OPERATION ( 1 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BELLIGERENCE ( 1 FDA reports)
BENIGN HEPATIC NEOPLASM ( 1 FDA reports)
BLADDER PAIN ( 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 BILIRUBIN DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 1 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BODY HEIGHT BELOW NORMAL ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIO-RESPIRATORY DISTRESS ( 1 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CERVICAL CYST ( 1 FDA reports)
CERVICAL DYSPLASIA ( 1 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 1 FDA reports)
CERVIX DISORDER ( 1 FDA reports)
CERVIX DYSTOCIA ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHEMICAL BURN OF SKIN ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CHOLECYSTOSTOMY ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
CLAVICLE FRACTURE ( 1 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 1 FDA reports)
COAGULATION TIME ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLONIC OBSTRUCTION ( 1 FDA reports)
COMPLICATION OF DELIVERY ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 1 FDA reports)
CONGENITAL MEGACOLON ( 1 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 1 FDA reports)
COOMBS NEGATIVE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
DANDY-WALKER SYNDROME ( 1 FDA reports)
DEAFNESS CONGENITAL ( 1 FDA reports)
DEFORMITY ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 1 FDA reports)
DEPERSONALISATION ( 1 FDA reports)
DEREALISATION ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DIVORCED ( 1 FDA reports)
DIVORCED PARENTS ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSTHYMIC DISORDER ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
EAR HAEMORRHAGE ( 1 FDA reports)
EAR MALFORMATION ( 1 FDA reports)
ECZEMA EYELIDS ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EOSINOPHILIC OESOPHAGITIS ( 1 FDA reports)
EPHELIDES ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
EPIPHYSEAL DISORDER ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 1 FDA reports)
EXERCISE LACK OF ( 1 FDA reports)
EXOPHTHALMOS ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
EXPOSURE VIA SEMEN ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE INFECTION BACTERIAL ( 1 FDA reports)
EYE INJURY ( 1 FDA reports)
EYELID CYST ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FAECES PALE ( 1 FDA reports)
FEAR OF DEATH ( 1 FDA reports)
FEELING GUILTY ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FEELINGS OF WORTHLESSNESS ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
FRUSTRATION ( 1 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 1 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 1 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 1 FDA reports)
GASTROINTESTINAL ULCER ( 1 FDA reports)
GENITAL BURNING SENSATION ( 1 FDA reports)
GENITAL DISORDER FEMALE ( 1 FDA reports)
GENITAL ULCERATION ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GRANULOMA ANNULARE ( 1 FDA reports)
GROWING PAINS ( 1 FDA reports)
HAEMATOSPERMIA ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMORRHAGIC CYST ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HLA MARKER STUDY POSITIVE ( 1 FDA reports)
HOMELESS ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
IMPATIENCE ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
INSULIN-LIKE GROWTH FACTOR INCREASED ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
IRITIS ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 1 FDA reports)
KERATOSIS PILARIS ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LACTOSE INTOLERANCE ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIP PAIN ( 1 FDA reports)
LIPOATROPHY ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
MACULAR HOLE ( 1 FDA reports)
MADAROSIS ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MANIA ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MEDULLOBLASTOMA ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MENOMETRORRHAGIA ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
MENSTRUATION DELAYED ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MONOCLONAL GAMMOPATHY ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MONONUCLEOSIS HETEROPHILE TEST POSITIVE ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MUSCLE STRAIN ( 1 FDA reports)
MUSCLE SWELLING ( 1 FDA reports)
MYCOTIC ALLERGY ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
NAIL INFECTION ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NECK MASS ( 1 FDA reports)
NO ADVERSE REACTION ( 1 FDA reports)
NODULE ON EXTREMITY ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OTITIS EXTERNA ( 1 FDA reports)
OTORRHOEA ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PAINFUL DEFAECATION ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PAPILLOMA VIRAL INFECTION ( 1 FDA reports)
PATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERIRECTAL ABSCESS ( 1 FDA reports)
PERIVENTRICULAR LEUKOMALACIA ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PHOBIA ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PITYRIASIS ROSEA ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMONIA VIRAL ( 1 FDA reports)
POLYCYSTIC OVARIES ( 1 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 1 FDA reports)
POSTOPERATIVE ILEUS ( 1 FDA reports)
PRECANCEROUS CELLS PRESENT ( 1 FDA reports)
PROCTOCOLITIS ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSYCHOLOGICAL ABUSE ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PUNCTATE KERATITIS ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
REACTION TO COLOURING ( 1 FDA reports)
RECTAL DISCHARGE ( 1 FDA reports)
RECTAL NEOPLASM ( 1 FDA reports)
RECTAL POLYP ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RETINAL TEAR ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RHABDOMYOSARCOMA ( 1 FDA reports)
RHINALGIA ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
SCHOOL REFUSAL ( 1 FDA reports)
SCROTAL SWELLING ( 1 FDA reports)
SELF ESTEEM DECREASED ( 1 FDA reports)
SELF MUTILATION ( 1 FDA reports)
SHOULDER DYSTOCIA ( 1 FDA reports)
SKIN DEPIGMENTATION ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN FRAGILITY ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SOCIAL PROBLEM ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
SPLENIC RUPTURE ( 1 FDA reports)
SPORTS INJURY ( 1 FDA reports)
STARING ( 1 FDA reports)
STEATORRHOEA ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STRESS FRACTURE ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
SUTURE INSERTION ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYNOVIAL DISORDER ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
THERMAL BURN ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 1 FDA reports)
TOOTH HYPOPLASIA ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO ABNORMAL ( 1 FDA reports)
TOURETTE'S DISORDER ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
UTERINE CERVIX ULCER ( 1 FDA reports)
UTERINE HAEMORRHAGE ( 1 FDA reports)
UVEITIS ( 1 FDA reports)
VASECTOMY ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VERBAL ABUSE ( 1 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
VIRAL PERICARDITIS ( 1 FDA reports)
VIRAL PHARYNGITIS ( 1 FDA reports)
VIRAL TEST POSITIVE ( 1 FDA reports)
VULVOVAGINAL DISCOMFORT ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)

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